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1. Nadezhdin, EV; Lebedev, YB; Glazkova, DV; Bornholdt, D; Arman, IP; Grzeschik, KH; Hunsmann, G; Sverdlov, ED
   Identification of paralogous HERV-K LTRs on human chromosomes 3, 4, 7 and 11 in regions containing clusters of olfactory receptor genes
   MOLECULAR GENETICS AND GENOMICS
   
   E.V. Nadezhdin et al., "Identification of paralogous HERV-K LTRs on human chromosomes 3, 4, 7 and 11 in regions containing clusters of olfactory receptor genes", MOL GENET G, 265(5), 2001, pp. 820-825
2. Stern, MC; Umbach, DM; van Gils, CH; Lunn, RM; Taylor, JA
   DNA repair gene XRCC1 polymorphisms, smoking, and bladder cancer risk
   CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
   
   M.C. Stern et al., "DNA repair gene XRCC1 polymorphisms, smoking, and bladder cancer risk", CANC EPID B, 10(2), 2001, pp. 125-131
3. Larkin, DM; Kuznetsov, SB; Astakhova, NM; Zhdanova, NS
   Using PCR markers for mapping pig chromosome 12
   RUSSIAN JOURNAL OF GENETICS
   
   D.M. Larkin et al., "Using PCR markers for mapping pig chromosome 12", RUSS J GEN, 37(3), 2001, pp. 276-282
4. Monnier, N; Romero, NB; Lerale, J; Landrieu, P; Nivoche, Y; Fardeau, M; Lunardi, J
   Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor
   HUMAN MOLECULAR GENETICS
   
   N. Monnier et al., "Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor", HUM MOL GEN, 10(22), 2001, pp. 2581-2592
5. Poduslo, SE; Yin, X
   A new locus on chromosome 19 linked with late-onset Alzheimer's disease
   NEUROREPORT
   
   S.E. Poduslo e X. Yin, "A new locus on chromosome 19 linked with late-onset Alzheimer's disease", NEUROREPORT, 12(17), 2001, pp. 3759-3761
6. Venanzi, S; Malerba, G; Galavotti, R; Lauciello, MC; Trabetti, E; Zanoni, G; Pescollderungg, L; Martinati, LC; Boner, AL; Pignatti, PF
   Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma
   CLINICAL AND EXPERIMENTAL ALLERGY
   
   S. Venanzi et al., "Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma", CLIN EXP AL, 31(8), 2001, pp. 1220-1224
7. Santos, J; Herranz, M; Fernandez, M; Vaquero, C; Lopez, P; Fernandez-Piqueras, J
   Evidence of a possible epigenetic inactivation mechanism operating on a region of mouse chromosome 19 in gamma-radiation-induced thymic lymphomas
   ONCOGENE
   
   J. Santos et al., "Evidence of a possible epigenetic inactivation mechanism operating on a region of mouse chromosome 19 in gamma-radiation-induced thymic lymphomas", ONCOGENE, 20(17), 2001, pp. 2186-2189
8. Kim, J; Gordon, L; Dehal, P; Badri, H; Christensen, M; Groza, M; Ha, C; Hammond, S; Vargas, M; Wehri, E; Wagner, M; Olsen, A; Stubbs, L
   Homology-driven assembly of a sequence-ready mouse BAC contig map spanningregions related to the 46-Mb gene-rich euchromatic segments of human chromosome 19
   GENOMICS
   
   J. Kim et al., "Homology-driven assembly of a sequence-ready mouse BAC contig map spanningregions related to the 46-Mb gene-rich euchromatic segments of human chromosome 19", GENOMICS, 74(2), 2001, pp. 129-141
9. Lagas, PA; Juvonen, V
   Schizophrenia in a patient with cerebral autosomally dominant arteriopathywith subcortical infarcts and leucoencephalopathy (CADASIL disease)
   NORDIC JOURNAL OF PSYCHIATRY
   
   P.A. Lagas e V. Juvonen, "Schizophrenia in a patient with cerebral autosomally dominant arteriopathywith subcortical infarcts and leucoencephalopathy (CADASIL disease)", NORD J PSY, 55(1), 2001, pp. 41-42
10. Zhou, GQ; Zhang, Y; Hammarstrom, S
    The carcinoembryonic antigen (CEA) gene family in non-human primates
    GENE
    
    G.Q. Zhou et al., "The carcinoembryonic antigen (CEA) gene family in non-human primates", GENE, 264(1), 2001, pp. 105-112
11. Yilmaz, F; Isbir, T; Agachan, B; Aydin, M
    Is epsilon 4 allele of apolipoprotein E associated with more severe end-organ damage in essential hypertension?
    CELL BIOCHEMISTRY AND FUNCTION
    
    F. Yilmaz et al., "Is epsilon 4 allele of apolipoprotein E associated with more severe end-organ damage in essential hypertension?", CELL BIOC F, 19(3), 2001, pp. 191-195
12. Vinogradova, TV; Leppik, LP; Nikolaev, LG; Akopov, SB; Kleiman, AM; Senyuta, NB; Sverdlov, ED
    Solitary human endogenous retroviruses-K LTRs retain transcriptional activity in vivo, the mode of which is different in different cell types
    VIROLOGY
    
    T.V. Vinogradova et al., "Solitary human endogenous retroviruses-K LTRs retain transcriptional activity in vivo, the mode of which is different in different cell types", VIROLOGY, 290(1), 2001, pp. 83-90
13. Burger, PC; Pearl, DK; Aldape, K; Yates, AJ; Scheithauer, BW; Passe, SM; Jenkins, RB; James, CD
    Small cell architecture - A histological equivalent of EGFR amplification in glioblastoma multiforme?
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    
    P.C. Burger et al., "Small cell architecture - A histological equivalent of EGFR amplification in glioblastoma multiforme?", J NE EXP NE, 60(11), 2001, pp. 1099-1104
14. Vargas, SO; French, CA; Faul, PN; Fletcher, JA; Davis, IJ; Dal Cin, P; Perez-Atayde, AR
    Upper respiratory tract carcinoma with chromosomal translocation 15;19 - Evidence for a distinct disease entity of young patients with a rapidly fatal course
    CANCER
    
    S.O. Vargas et al., "Upper respiratory tract carcinoma with chromosomal translocation 15;19 - Evidence for a distinct disease entity of young patients with a rapidly fatal course", CANCER, 92(5), 2001, pp. 1195-1203
15. Takashima, H; Nishio, H; Wakao, H; Nishio, M; Koizumi, K; Oda, A; Koike, T; Sawada, K
    Molecular cloning and characterization of a KRAB-containing zinc finger protein, ZNF317, and its isoforms
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    
    H. Takashima et al., "Molecular cloning and characterization of a KRAB-containing zinc finger protein, ZNF317, and its isoforms", BIOC BIOP R, 288(4), 2001, pp. 771-779
16. Yousef, GM; Bharaj, BS; Yu, H; Poulopoulos, J; Diamandis, EP
    Sequence analysis of the human kallikrein gene locus identifies a unique polymorphic minisatellite element
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    
    G.M. Yousef et al., "Sequence analysis of the human kallikrein gene locus identifies a unique polymorphic minisatellite element", BIOC BIOP R, 285(5), 2001, pp. 1321-1329
17. Yamawaki, K; Ito, M; Machida, H; Moriki, N; Okamoto, R; Isaka, N; Shimpo, H; Kohda, A; Okumura, K; Hartshorne, DJ; Nakano, T
    Identification of human CPI-17, an inhibitory phosphoprotein for myosin phosphatase
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    
    K. Yamawaki et al., "Identification of human CPI-17, an inhibitory phosphoprotein for myosin phosphatase", BIOC BIOP R, 285(4), 2001, pp. 1040-1045
18. Scimeca, JC; Franchi, A; Trojani, C; Parrinello, H; Grosgeorge, J; Robert, C; Jaillon, O; Poirier, C; Gaudray, P; Carle, GF
    The gene encoding the mouse homologue of the human osteoclast-specific 116-kDa V-ATPase subunit bears a deletion in osteosclerotic (oc/oc) mutants
    BONE
    
    J.C. Scimeca et al., "The gene encoding the mouse homologue of the human osteoclast-specific 116-kDa V-ATPase subunit bears a deletion in osteosclerotic (oc/oc) mutants", BONE, 26(3), 2000, pp. 207-213
19. D'Alfonso, S; Nistico, L; Bocchio, D; Bomprezzi, R; Marrosu, MG; Murru, MR; Lai, M; Massacesi, L; Ballerini, C; Repice, A; Salvetti, M; Montesperelli, C; Ristori, G; Trojano, M; Liguori, M; Gambi, D; Quattrone, A; Tosi, R; Momigliano-Richiardi, P
    An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population
    JOURNAL OF NEUROVIROLOGY
    
    S. D'Alfonso et al., "An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population", J NEUROVIRO, 6, 2000, pp. S18-S22
20. Puttagunta, R; Gordon, LA; Meyer, GE; Kapfhamer, D; Lamerdin, JE; Kantheti, P; Portman, KM; Chung, WK; Jenne, DE; Olsen, AS; Burmeister, M
    Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints
    GENOME RESEARCH
    
    R. Puttagunta et al., "Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints", GENOME RES, 10(9), 2000, pp. 1369-1380
21. Kipnes, JR; Xu, L; Han, F; Rallapalli, R; Jimenez, S; Hall, DJ; Tuan, RS; Li, Y
    Molecular cloning and expression patterns of mouse cartilage oligomeric matrix protein gene
    OSTEOARTHRITIS AND CARTILAGE
    
    J.R. Kipnes et al., "Molecular cloning and expression patterns of mouse cartilage oligomeric matrix protein gene", OSTEO CART, 8(3), 2000, pp. 236-239
22. Sangiuolo, F; Bruscia, E; Capon, F; Servidei, S; Dallapiccola, B; Novelli, G
    Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3
    EUROPEAN JOURNAL OF HUMAN GENETICS
    
    F. Sangiuolo et al., "Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3", EUR J HUM G, 8(10), 2000, pp. 809-812
23. Romagno, D; Chiarelli, B; Guarducci, S; Uziella, MLG; Sineo, L
    Chromosome mapping of GABRB3 and PML loci in Macaca and Cercopithecus indicates the mechanism of evolution of human chromosome 15
    CHROMOSOME RESEARCH
    
    D. Romagno et al., "Chromosome mapping of GABRB3 and PML loci in Macaca and Cercopithecus indicates the mechanism of evolution of human chromosome 15", CHROMOS RES, 8(8), 2000, pp. 747-749
24. Catalan, J; Auffray, JC; Pellestor, F; Britton-Davidian, J
    Spontaneous occurrence of a Robertsonian fusion involving chromosome 19 bysingle whole-arm reciprocal translocation (WART) in wild-derived house mice
    CHROMOSOME RESEARCH
    
    J. Catalan et al., "Spontaneous occurrence of a Robertsonian fusion involving chromosome 19 bysingle whole-arm reciprocal translocation (WART) in wild-derived house mice", CHROMOS RES, 8(7), 2000, pp. 593-601
25. Eilertsen, KJ; Tran, T; Sundberg, JP; Stenn, KS; Parimoo, S
    High resolution genetic and physical mapping of the mouse asebia locus: A key gene locus for sebaceous gland differentiation
    JOURNAL OF EXPERIMENTAL ANIMAL SCIENCE
    
    K.J. Eilertsen et al., "High resolution genetic and physical mapping of the mouse asebia locus: A key gene locus for sebaceous gland differentiation", J EXP ANIM, 40(4), 2000, pp. 165-170
26. Wada, H
    Analyses of serum concentrations of apolipoproteins in the demented elderly
    INTERNAL MEDICINE
    
    H. Wada, "Analyses of serum concentrations of apolipoproteins in the demented elderly", INTERN MED, 39(3), 2000, pp. 220-222
27. Lebedev, YB; Belonovitch, OS; Zybrova, NV; Khil, PP; Kurdyukov, SG; Vinogradova, TV; Hunsmann, G; Sverdlov, ED
    Differences in HERV-K LTR insertions in orthologous loci of humans and great apes
    GENE
    
    Y.B. Lebedev et al., "Differences in HERV-K LTR insertions in orthologous loci of humans and great apes", GENE, 247(1-2), 2000, pp. 265-277
28. Scott, DA; Drury, S; Sundstrom, RA; Bishop, J; Swiderski, RE; Carmi, R; Ramesh, A; Elbedour, K; Srisailapathy, CRS; Keats, BJ; Sheffield, VC; Smith, RJH
    Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms ina novel gene, TMEM2
    GENE
    
    D.A. Scott et al., "Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms ina novel gene, TMEM2", GENE, 246(1-2), 2000, pp. 265-274
29. Kurkinen, KMA; Keinanen, RA; Karhu, R; Koistinaho, J
    Genomic structure and chromosomal localization of the rat protein kinase Cdelta-gene
    GENE
    
    K.M.A. Kurkinen et al., "Genomic structure and chromosomal localization of the rat protein kinase Cdelta-gene", GENE, 242(1-2), 2000, pp. 115-123
30. Medica, I; Logar, N; Peterlin, B
    Characteristics of myotonic dystrophy in Istria: Molecular genetic approach. Part II: Analysis of genetic polymorphisms
    COLLEGIUM ANTROPOLOGICUM
    
    I. Medica et al., "Characteristics of myotonic dystrophy in Istria: Molecular genetic approach. Part II: Analysis of genetic polymorphisms", COLL ANTROP, 24(2), 2000, pp. 287-294
31. Nakauchi, J; Matsuo, H; Kim, DK; Goto, A; Chairoungdua, A; Cha, SH; Inatomi, J; Shiokawa, Y; Yamaguchi, K; Saito, I; Endou, H; Kanai, Y
    Cloning and characterization of a human brain Na+-independent transporter for small neutral amino acids that transports D-serine with high affinity
    NEUROSCIENCE LETTERS
    
    J. Nakauchi et al., "Cloning and characterization of a human brain Na+-independent transporter for small neutral amino acids that transports D-serine with high affinity", NEUROSCI L, 287(3), 2000, pp. 231-235
32. Bielec, P; Gallagher, D; Yang, YP; Womack, J; Davis, S; Taylor, J; Busbee, D
    Assignment of crystallin beta-polypeptide 1 (CRYBA1) to Atlantic bottlenose dolphin chromosome band 16p11 by in situ hybridization
    CYTOGENETICS AND CELL GENETICS
    
    P. Bielec et al., "Assignment of crystallin beta-polypeptide 1 (CRYBA1) to Atlantic bottlenose dolphin chromosome band 16p11 by in situ hybridization", CYTOG C GEN, 89(1-2), 2000, pp. 96-97
33. LaPlante, JM; O'Rourke, F; Lu, XH; Fein, A; Olsen, A; Feinstein, MB
    Cloning of human Ca2+ homoeostasis endoplasmic reticulum protein (CHERP): regulated expression of antisense cDNA depletes CHERP, inhibits intracellular Ca2+ mobilization and decreases cell proliferation
    BIOCHEMICAL JOURNAL
    
    J.M. LaPlante et al., "Cloning of human Ca2+ homoeostasis endoplasmic reticulum protein (CHERP): regulated expression of antisense cDNA depletes CHERP, inhibits intracellular Ca2+ mobilization and decreases cell proliferation", BIOCHEM J, 348, 2000, pp. 189-199
34. Bello, MJ; de Campos, JM; Vaquero, J; Ruiz-Barnes, P; Kusak, ME; Sarasa, JL; Rey, JA
    hRAD54 gene and 1p high-resolution deletion-mapping analyses in oligodendrogliomas
    CANCER GENETICS AND CYTOGENETICS
    
    M.J. Bello et al., "hRAD54 gene and 1p high-resolution deletion-mapping analyses in oligodendrogliomas", CANC GENET, 116(2), 2000, pp. 142-147
35. Bhat, M; Morrison, PJ; Getty, A; McManus, D; Tubman, R; Nevin, NC
    First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH
    AMERICAN JOURNAL OF MEDICAL GENETICS
    
    M. Bhat et al., "First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH", AM J MED G, 91(3), 2000, pp. 201-203
36. Liu, WR; Kim, J; Nwankwo, C; Ashworth, LK; Arm, JP
    Genomic organization of the human leukocyte immunoglobulin-like receptors within the leukocyte receptor complex on Chromosome 19q13.4
    IMMUNOGENETICS
    
    W.R. Liu et al., "Genomic organization of the human leukocyte immunoglobulin-like receptors within the leukocyte receptor complex on Chromosome 19q13.4", IMMUNOGENET, 51(8-9), 2000, pp. 659-669
37. Scacheri, PC; Hoffman, EP; Fratkin, JD; Semino-Mora, C; Senchak, A; Davis, MR; Laing, NG; Vedanarayanan, V; Subramony, SH
    A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathy
    NEUROLOGY
    
    P.C. Scacheri et al., "A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathy", NEUROLOGY, 55(11), 2000, pp. 1689-1696
38. Nakamura, M; Yang, F; Fujisawa, H; Yonekawa, Y; Kleihues, P; Ohgaki, H
    Loss of heterozygosity on chromosome 19 in secondary glioblastomas
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    
    M. Nakamura et al., "Loss of heterozygosity on chromosome 19 in secondary glioblastomas", J NE EXP NE, 59(6), 2000, pp. 539-543
39. Brito, RM; Ribeiro, T; Viriato, L; Vieira-Silva, C; Espinheira, R; Pinto-Ribeiro, I; Geada, H
    Sequence variation of new alleles at the short tandem repeat D19S253 locus
    JOURNAL OF FORENSIC SCIENCES
    
    R.M. Brito et al., "Sequence variation of new alleles at the short tandem repeat D19S253 locus", J FOREN SCI, 45(4), 2000, pp. 932-934
40. Berghs, S; Aggujaro, D; Dirkx, R; Maksimova, E; Stabach, P; Hermel, JM; Zhang, JP; Philbrick, W; Slepnev, V; Ort, T; Solimena, M
    beta IV spectrin, a new spectrin localized at axon initial segments and nodes of ranvier in the central and peripheral nervous system
    JOURNAL OF CELL BIOLOGY
    
    S. Berghs et al., "beta IV spectrin, a new spectrin localized at axon initial segments and nodes of ranvier in the central and peripheral nervous system", J CELL BIOL, 151(5), 2000, pp. 985-1001
41. Domansky, AN; Kopantzev, EP; Snezhkov, EV; Lebedev, YB; Leib-Mosch, C; Sverdlov, ED
    Solitary HERV-K LTRs possess bi-directional promoter activity and contain a negative regulatory element in the U5 region
    FEBS LETTERS
    
    A.N. Domansky et al., "Solitary HERV-K LTRs possess bi-directional promoter activity and contain a negative regulatory element in the U5 region", FEBS LETTER, 472(2-3), 2000, pp. 191-195
42. Mugneret, F; Chaffanet, M; Maynadie, M; Guasch, G; Favre, B; Casasnovas, O; Birnbaum, D; Pebusque, MJ
    The 8p12 myeloproliferative disorder. t(8;19)(p12;q13.3): a novel translocation involving the FGFR1 gene
    BRITISH JOURNAL OF HAEMATOLOGY
    
    F. Mugneret et al., "The 8p12 myeloproliferative disorder. t(8;19)(p12;q13.3): a novel translocation involving the FGFR1 gene", BR J HAEM, 111(2), 2000, pp. 647-649
43. Yousef, GM; Chang, A; Scorilas, A; Diamandis, EP
    Genomic organization of the human kallikrein gene family on chromosome 19q13.3-q13.4
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    
    G.M. Yousef et al., "Genomic organization of the human kallikrein gene family on chromosome 19q13.3-q13.4", BIOC BIOP R, 276(1), 2000, pp. 125-133
44. Larkin, DM; Serov, OL; Zhdanova, NS
    Mapping of five genes from human chromosome 17 to chromosome hn of the common shrew Sorex araneus
    ACTA THERIOLOGICA
    
    D.M. Larkin et al., "Mapping of five genes from human chromosome 17 to chromosome hn of the common shrew Sorex araneus", ACT THERIOL, 45, 2000, pp. 143-146
45. Rippe, V; Belge, G; Meiboom, M; Kazmierczak, B; Fusco, A; Bullerdiek, J
    A KRAB zinc finger protein gene is the potential target of 19q13 translocation in benign thyroid tumors
    GENES CHROMOSOMES & CANCER
    
    V. Rippe et al., "A KRAB zinc finger protein gene is the potential target of 19q13 translocation in benign thyroid tumors", GENE CHROM, 26(3), 1999, pp. 229-236
46. Smith, JS; Alderete, B; Minn, Y; Borell, TJ; Perry, A; Mohapatra, G; Hosek, SM; Kimmel, D; O'Fallon, J; Yates, A; Feuerstein, BG; Burger, PC; Scheithauer, BW; Jenkins, RB
    Localization of common deletion regions on 1p and 19q in human gliomas andtheir association with histological subtype
    ONCOGENE
    
    J.S. Smith et al., "Localization of common deletion regions on 1p and 19q in human gliomas andtheir association with histological subtype", ONCOGENE, 18(28), 1999, pp. 4144-4152
47. Ji, WZ; Herron, B; Jones, JM; Jenkins, NA; Gilbert, DJ; Copeland, NG; Swank, R; Flaherty, L; Meisler, MH
    Identification of genes within the Krd deletion on mouse chromosome 19
    MAMMALIAN GENOME
    
    W.Z. Ji et al., "Identification of genes within the Krd deletion on mouse chromosome 19", MAMM GENOME, 10(4), 1999, pp. 399-401
48. Li, HZ; Wu, DK; Sullivan, SL
    Characterization and expression of sema4g, a novel member of the semaphorin gene family
    MECHANISMS OF DEVELOPMENT
    
    H.Z. Li et al., "Characterization and expression of sema4g, a novel member of the semaphorin gene family", MECH DEVEL, 87(1-2), 1999, pp. 169-173
49. Sullivan, M; Olsen, AS; Houslay, MD
    Genomic organisation of the human cyclic AMP-specific phosphodiesterase PDE4C gene and its chromosomal localisation to 19p13.1, between RAB3A and JUND
    CELLULAR SIGNALLING
    
    M. Sullivan et al., "Genomic organisation of the human cyclic AMP-specific phosphodiesterase PDE4C gene and its chromosomal localisation to 19p13.1, between RAB3A and JUND", CELL SIGNAL, 11(10), 1999, pp. 735-742
50. Feliubadalo, L; Bisceglia, L; Font, M; Dello Strologo, L; Beccia, E; Arslan-Kirchner, M; Steinmann, B; Zelante, L; Estivill, X; Zorzano, A; Palacin, M; Gasparini, P; Nunes, V
    Recombinant families locate the gene for non-type I cystinuria between markers C13 and D19S587 on chromosome 19q13.1
    GENOMICS
    
    L. Feliubadalo et al., "Recombinant families locate the gene for non-type I cystinuria between markers C13 and D19S587 on chromosome 19q13.1", GENOMICS, 60(3), 1999, pp. 362-365
51. Pras, E; Pras, E; Kreiss, Y; Frishberg, Y; Prosen, L; Aksentijevich, I; Kastner, DL
    Refined mapping of the CSNU3 gene to a 1.8-Mb region on chromosome 19q13.1using historical recombinants in libyan Jewish cystinuria patients
    GENOMICS
    
    E. Pras et al., "Refined mapping of the CSNU3 gene to a 1.8-Mb region on chromosome 19q13.1using historical recombinants in libyan Jewish cystinuria patients", GENOMICS, 60(2), 1999, pp. 248-250
52. Higa, S; Yoshihama, M; Tanaka, T; Kenmochi, N
    Gene organization and sequence of the region containing the ribosomal protein genes RPL13A and RPS11 in the human genome and conserved features in the mouse genome
    GENE
    
    S. Higa et al., "Gene organization and sequence of the region containing the ribosomal protein genes RPL13A and RPS11 in the human genome and conserved features in the mouse genome", GENE, 240(2), 1999, pp. 371-377
53. Frants, RR
    The use of isolates in migraine genetic research
    CEPHALALGIA
    
    R.R. Frants, "The use of isolates in migraine genetic research", CEPHALALGIA, 19, 1999, pp. 19-24
54. Kim, HS; Wadekar, RV; Takenaka, O; Hyun, BH; Crow, TJ
    Phylogenetic analysis of HERV-K LTR-like elements in primates: presence insome New World monkeys and evidence of recent parallel evolution in these species and in Homo sapiens
    ARCHIVES OF VIROLOGY
    
    H.S. Kim et al., "Phylogenetic analysis of HERV-K LTR-like elements in primates: presence insome New World monkeys and evidence of recent parallel evolution in these species and in Homo sapiens", ARCH VIROL, 144(10), 1999, pp. 2035-2040
55. Iannuzzi, L; Gallagher, DS; Di Meo, GP; Yang, Y; Womack, JE; Davis, SK; Taylor, JF
    Comparative FISH-mapping of six expressed gene loci to river buffalo and sheep chromosomes
    CYTOGENETICS AND CELL GENETICS
    
    L. Iannuzzi et al., "Comparative FISH-mapping of six expressed gene loci to river buffalo and sheep chromosomes", CYTOG C GEN, 84(3-4), 1999, pp. 161-163
56. Gao, AC; Lou, W; Ichikawa, T; Denmeade, SR; Barrett, JC; Isaacs, JT
    Suppression of the tumorigenicity of prostatic cancer cells by gene(s) located on human chromosome 19p13.1-13.2
    PROSTATE
    
    A.C. Gao et al., "Suppression of the tumorigenicity of prostatic cancer cells by gene(s) located on human chromosome 19p13.1-13.2", PROSTATE, 38(1), 1999, pp. 46-54
57. Ludwig, A; Zong, XG; Stieber, J; Hullin, R; Hofmann, F; Biel, M
    Two pacemaker channels from human heart with profoundly different activation kinetics
    EMBO JOURNAL
    
    A. Ludwig et al., "Two pacemaker channels from human heart with profoundly different activation kinetics", EMBO J, 18(9), 1999, pp. 2323-2329
58. Rivera, MA; Perusse, L; Simoneau, JA; Gagnon, J; Dionne, FT; Leon, AS; Skinner, JS; Wilmore, JH; Province, M; Rao, DC; Bouchard, C
    Linkage between a muscle-specific CK gene marker and VO2max in the HERITAGE Family Study
    MEDICINE AND SCIENCE IN SPORTS AND EXERCISE
    
    M.A. Rivera et al., "Linkage between a muscle-specific CK gene marker and VO2max in the HERITAGE Family Study", MED SCI SPT, 31(5), 1999, pp. 698-701
59. Vaccari, T; Moroni, A; Rocchi, M; Gorza, L; Bianchi, ME; Beltrame, M; DiFrancesco, D
    The human gene coding for HCN2, a pacemaker channel of the heart
    BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    
    T. Vaccari et al., "The human gene coding for HCN2, a pacemaker channel of the heart", BBA-GENE ST, 1446(3), 1999, pp. 419-425
60. Magnani, I; Chiariello, E; Conti, AMF; Finocchiaro, G
    A recurrent 19q11-12 breakpoint suggested by cytogenetic and fluorescence in situ hybridization analysis of three glioblastoma cell lines
    CANCER GENETICS AND CYTOGENETICS
    
    I. Magnani et al., "A recurrent 19q11-12 breakpoint suggested by cytogenetic and fluorescence in situ hybridization analysis of three glioblastoma cell lines", CANC GENET, 110(2), 1999, pp. 82-86
61. Chernov, IP; Polyakov, AS; Akopov, SB; Nikolaev, LG; Azhikina, TL; Kostina, MB; Sverdlov, ED
    Identification and human chromosome 19 mapping of a chromosome-specific repeated element binding preferentially to nuclear matrix
    BIOORGANICHESKAYA KHIMIYA
    
    I.P. Chernov et al., "Identification and human chromosome 19 mapping of a chromosome-specific repeated element binding preferentially to nuclear matrix", BIOORG KHIM, 25(4), 1999, pp. 275-281
62. Berg, SF; Westgaard, IH; Fossum, S; Dissen, E
    A rat gene homologous to human granule membrane protein 17 is expressed bynatural killer cells, CD8(+) T cells, and a mast cell line
    IMMUNOGENETICS
    
    S.F. Berg et al., "A rat gene homologous to human granule membrane protein 17 is expressed bynatural killer cells, CD8(+) T cells, and a mast cell line", IMMUNOGENET, 49(9), 1999, pp. 815-818
63. Kraimps, JL; Canzian, F; Jost, C; Menet, E; Amati, P; Levillian, P; Harach, R; Lesueur, F; Barbier, J; Romeo, G; Bonneau, D
    Mapping of a gene predisposing to familial thyroid tumors with cell oxyphilia to chromosome 19 and exclusion of JUN B as a candidate gene
    SURGERY
    
    J.L. Kraimps et al., "Mapping of a gene predisposing to familial thyroid tumors with cell oxyphilia to chromosome 19 and exclusion of JUN B as a candidate gene", SURGERY, 126(6), 1999, pp. 1188-1194
64. Murphy, C
    Loss of olfactory function in dementing disease
    PHYSIOLOGY & BEHAVIOR
    
    C. Murphy, "Loss of olfactory function in dementing disease", PHYSL BEHAV, 66(2), 1999, pp. 177-182
65. Rasko, JEJ; Battini, JL; Gottschalk, RJ; Mazo, I; Miller, AD
    The RD114 simian type D retrovirus receptor is a neutral amino acid transporter
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    
    J.E.J. Rasko et al., "The RD114 simian type D retrovirus receptor is a neutral amino acid transporter", P NAS US, 96(5), 1999, pp. 2129-2134
66. Lapuk, AV; Khil, PP; Lavrentieva, IV; Lebedev, YB; Sverdlov, ED
    A human endogenous retrovirus-like (HERV) LTR formed more than 10 million years ago due to an insertion of HERV-H LTR into the 5 ' LTR of HERV-K is situated on human chromosomes 10, 19 and Y
    JOURNAL OF GENERAL VIROLOGY
    
    A.V. Lapuk et al., "A human endogenous retrovirus-like (HERV) LTR formed more than 10 million years ago due to an insertion of HERV-H LTR into the 5 ' LTR of HERV-K is situated on human chromosomes 10, 19 and Y", J GEN VIROL, 80, 1999, pp. 835-839
67. Jilani, A; Ramotar, D; Slack, C; Ong, C; Yang, XM; Scherer, SW; Lasko, DD
    Molecular cloning of the human gene, PNKP, encoding a polynucleotide kinase 3 '-phosphatase and evidence for its role in repair of DNA strand breaks caused by oxidative damage
    JOURNAL OF BIOLOGICAL CHEMISTRY
    
    A. Jilani et al., "Molecular cloning of the human gene, PNKP, encoding a polynucleotide kinase 3 '-phosphatase and evidence for its role in repair of DNA strand breaks caused by oxidative damage", J BIOL CHEM, 274(34), 1999, pp. 24176-24186
68. Kozyrev, SV; Hansen, LL; Poltaraus, AB; Domninsky, DA; Kisselev, LL
    Structure of the human CpG-island-containing lung Kruppel-like factor (LKLF) gene and its location in chromosome 19p13.11-13 locus
    FEBS LETTERS
    
    S.V. Kozyrev et al., "Structure of the human CpG-island-containing lung Kruppel-like factor (LKLF) gene and its location in chromosome 19p13.11-13 locus", FEBS LETTER, 448(1), 1999, pp. 149-152
69. Orho-Melander, M; Almgren, P; Kanninen, T; Forsblom, C; Groop, LC
    A paired-sibling analysis of the Xbal polymorphism in the muscle glycogen synthase gene
    DIABETOLOGIA
    
    M. Orho-Melander et al., "A paired-sibling analysis of the Xbal polymorphism in the muscle glycogen synthase gene", DIABETOLOG, 42(9), 1999, pp. 1138-1145
70. Ramenghi, U; Garelli, E; Valtolina, S; Campagnoli, MF; Timeus, F; Crescenzio, N; Mair, M; Varotto, S; D'Avanzo, M; Nobili, B; Massolo, F; Mori, PG; Locatelli, F; Gustavsson, P; Dahl, N; Dianzani, I
    Diamond-Blackfan anaemia in the Italian population
    BRITISH JOURNAL OF HAEMATOLOGY
    
    U. Ramenghi et al., "Diamond-Blackfan anaemia in the Italian population", BR J HAEM, 104(4), 1999, pp. 841-848
71. Bigner, SH; Matthews, MR; Rasheed, BKA; Wiltshire, RN; Friedman, HS; Friedman, AH; Stenzel, TT; Dawes, DM; McLendon, RE; Bigner, DD
    Molecular genetic aspects of oligodendrogliomas including analysis by comparative genomic hybridization
    AMERICAN JOURNAL OF PATHOLOGY
    
    S.H. Bigner et al., "Molecular genetic aspects of oligodendrogliomas including analysis by comparative genomic hybridization", AM J PATH, 155(2), 1999, pp. 375-386
72. Slot, F; Olsen, AS; Rao, PN; Abraham, CR
    Localization of human endopeptidase EC 3.4.24.15 (THOP1) to chromosome 19p13.3
    ALZHEIMERS REPORTS
    
    F. Slot et al., "Localization of human endopeptidase EC 3.4.24.15 (THOP1) to chromosome 19p13.3", ALZHEIM REP, 1(5), 1998, pp. 327-331
73. LOUGHLIN J; IRVEN C; MUSTAFA Z; BRIGGS MD; CARR A; LYNCH SA; KNOWLTON RG; COHN DH; SYKES B
    IDENTIFICATION OF 5 NOVEL MUTATIONS IN CARTILAGE OLIGOMERIC MATRIX PROTEIN GENE IN PSEUDOACHRONDROPLASIA AND MULTIPLE EPIPHYSEAL DYSPLASIA
    Human mutation
    
    J. Loughlin et al., "IDENTIFICATION OF 5 NOVEL MUTATIONS IN CARTILAGE OLIGOMERIC MATRIX PROTEIN GENE IN PSEUDOACHRONDROPLASIA AND MULTIPLE EPIPHYSEAL DYSPLASIA", Human mutation, 1998, pp. 10-17
74. Ollendorff, V; Mattei, MG; Fournier, E; Adelaide, J; Lopez, M; Rosnet, O; Birnbaum, D
    A third human CBL gene is on chromosome 19
    INTERNATIONAL JOURNAL OF ONCOLOGY
    
    V. Ollendorff et al., "A third human CBL gene is on chromosome 19", INT J ONCOL, 13(6), 1998, pp. 1159-1161
75. JOHNSON EW; DUBOVSKY J; RICH SS; ODONOVAN CA; ORR HT; ANDERSON VE; GILNAGEL A; AHMANN P; DOKKEN CG; SCHNEIDER DT; WEBER JL
    EVIDENCE FOR A NOVEL GENE FOR FAMILIAL FEBRILE CONVULSIONS, FEB2, LINKED TO CHROMOSOME 19P IN AN EXTENDED FAMILY FROM THE MIDWEST
    Human molecular genetics
    
    E.W. Johnson et al., "EVIDENCE FOR A NOVEL GENE FOR FAMILIAL FEBRILE CONVULSIONS, FEB2, LINKED TO CHROMOSOME 19P IN AN EXTENDED FAMILY FROM THE MIDWEST", Human molecular genetics, 7(1), 1998, pp. 63-67
76. CARVER EA; ISSELTARVER L; RINE J; OLSEN AS; STUBBS L
    LOCATION OF MOUSE AND HUMAN GENES CORRESPONDING TO CONSERVED CANINE OLFACTORY RECEPTOR GENE SUBFAMILIES
    Mammalian genome
    
    E.A. Carver et al., "LOCATION OF MOUSE AND HUMAN GENES CORRESPONDING TO CONSERVED CANINE OLFACTORY RECEPTOR GENE SUBFAMILIES", Mammalian genome, 9(5), 1998, pp. 349-354
77. VINAS AM; DRURY SS; DEANGELIS MM; DEN ZI; HUANG JM; BERLIN CI; HUNT JD; BATZER MA; DENINGER PL; KEATS BJB
    THE MOUSE DEAFNESS LOCUS (DN) IS ASSOCIATED WITH AN INVERSION ON CHROMOSOME-19
    Biochimica et biophysica acta. Molecular basis of disease
    
    A.M. Vinas et al., "THE MOUSE DEAFNESS LOCUS (DN) IS ASSOCIATED WITH AN INVERSION ON CHROMOSOME-19", Biochimica et biophysica acta. Molecular basis of disease, 1407(3), 1998, pp. 257-262
78. MOHRENWEISER HW; TSUJIMOTO S; GORDON L; OLSEN AS
    REGIONS OF SEX-SPECIFIC HYPO-RECOMBINATION AND HYPER-RECOMBINATION IDENTIFIED THROUGH INTEGRATION OF 180 GENETIC-MARKERS INTO THE METRIC PHYSICAL MAP OF HUMAN-CHROMOSOME-19
    Genomics
    
    H.W. Mohrenweiser et al., "REGIONS OF SEX-SPECIFIC HYPO-RECOMBINATION AND HYPER-RECOMBINATION IDENTIFIED THROUGH INTEGRATION OF 180 GENETIC-MARKERS INTO THE METRIC PHYSICAL MAP OF HUMAN-CHROMOSOME-19", Genomics, 47(2), 1998, pp. 153-162
79. NIKOLAEV LG; AKOPOV SB; CHERNOV IP; GLOTOV BO; ASHWORTH LK; SVERDLOV ED
    POSITION OF 19 NUCLEAR MATRIX ASSOCIATED REGIONS (MARS) ON HUMAN-CHROMOSOME-19
    Doklady Akademii nauk. Rossijskaa akademia nauk
    
    L.G. Nikolaev et al., "POSITION OF 19 NUCLEAR MATRIX ASSOCIATED REGIONS (MARS) ON HUMAN-CHROMOSOME-19", Doklady Akademii nauk. Rossijskaa akademia nauk, 361(3), 1998, pp. 409-411
80. KUGLER SL; JOHNSON WG
    GENETICS OF THE FEBRILE SEIZURE SUSCEPTIBILITY TRAIT
    Brain & development
    
    S.L. Kugler e W.G. Johnson, "GENETICS OF THE FEBRILE SEIZURE SUSCEPTIBILITY TRAIT", Brain & development, 20(5), 1998, pp. 265-274
81. LENKKERI U; KESTILA M; LAMERDIN J; MCCREADY P; ADAMSON A; OLSEN A; TRYGGVASON K
    STRUCTURE OF THE HUMAN AMYLOID-PRECURSOR-LIKE PROTEIN GENE APLP1 AT 19Q13.1
    Human genetics
    
    U. Lenkkeri et al., "STRUCTURE OF THE HUMAN AMYLOID-PRECURSOR-LIKE PROTEIN GENE APLP1 AT 19Q13.1", Human genetics, 102(2), 1998, pp. 192-196
82. Ikegawa, S; Ohashi, H; Nishimura, G; Kim, KC; Sannohe, A; Kimizuka, M; Fukushima, Y; Nagai, T; Nakamura, Y
    Novel and recurrent COMP (cartilage oligomeric matrix protein) mutations in pseudoachondroplasia and multiple epiphyseal dysplasia
    HUMAN GENETICS
    
    S. Ikegawa et al., "Novel and recurrent COMP (cartilage oligomeric matrix protein) mutations in pseudoachondroplasia and multiple epiphyseal dysplasia", HUM GENET, 103(6), 1998, pp. 633-638
83. KLINOV DV; LAGUTINA IV; PROKHOROV VV; NERETINA T; KHIL PP; LEBEDEV YB; CHERNY DI; DEMIN VV; SVERDLOV ED
    HIGH-RESOLUTION MAPPING DNAS BY R-LOOP ATOMIC-FORCE MICROSCOPY
    Nucleic acids research
    
    D.V. Klinov et al., "HIGH-RESOLUTION MAPPING DNAS BY R-LOOP ATOMIC-FORCE MICROSCOPY", Nucleic acids research, 26(20), 1998, pp. 4603-4610
84. SHINKAI T; OHMORI O; KOJIMA H; TERAO T; SUZUKI T; ABE K; NAKAMURA J
    APOLIPOPROTEIN-E REGULATORY REGION GENOTYPE IN SCHIZOPHRENIA
    Neuroscience letters
    
    T. Shinkai et al., "APOLIPOPROTEIN-E REGULATORY REGION GENOTYPE IN SCHIZOPHRENIA", Neuroscience letters, 256(1), 1998, pp. 57-60
85. VANMOURIK JBA; BUMA P; WILCOX WR
    ELECTRON-MICROSCOPIC STUDY IN MULTIPLE EPIPHYSEAL DYSPLASIA TYPE-II
    Ultrastructural pathology
    
    J.B.A. Vanmourik et al., "ELECTRON-MICROSCOPIC STUDY IN MULTIPLE EPIPHYSEAL DYSPLASIA TYPE-II", Ultrastructural pathology, 22(3), 1998, pp. 249-251
86. KUGLER SL; STENROOS ES; MANDELBAUM DE; LEHNER T; MCKOY VV; PROSSICK T; SASVARI J; SWANNICK K; KATZ J; JOHNSON WG
    HEREDITARY FEBRILE SEIZURES - PHENOTYPE AND EVIDENCE FOR A CHROMOSOME19P LOCUS
    American journal of medical genetics
    
    S.L. Kugler et al., "HEREDITARY FEBRILE SEIZURES - PHENOTYPE AND EVIDENCE FOR A CHROMOSOME19P LOCUS", American journal of medical genetics, 79(5), 1998, pp. 354-361
87. KULHARYA AS; MICHAELIS RC; NORRIS KS; TAYLOR HA; GARCIAHERAS J
    CONSTITUTIONAL DEL(19)(Q12Q13.1) IN A 3-YEAR-OLD GIRL WITH SEVERE PHENOTYPIC ABNORMALITIES AFFECTING MULTIPLE ORGAN SYSTEMS
    American journal of medical genetics
    
    A.S. Kulharya et al., "CONSTITUTIONAL DEL(19)(Q12Q13.1) IN A 3-YEAR-OLD GIRL WITH SEVERE PHENOTYPIC ABNORMALITIES AFFECTING MULTIPLE ORGAN SYSTEMS", American journal of medical genetics, 77(5), 1998, pp. 391-394
88. Deere, M; Sanford, T; Ferguson, HL; Daniels, K; Hecht, JT
    Identification of twelve mutations in cartilage oligomeric matrix protein (COMP) in patients with pseudoachondroplasia
    AMERICAN JOURNAL OF MEDICAL GENETICS
    
    M. Deere et al., "Identification of twelve mutations in cartilage oligomeric matrix protein (COMP) in patients with pseudoachondroplasia", AM J MED G, 80(5), 1998, pp. 510-513
89. KHIL PP; LEBEDEV YB; SVERDLOV ED
    THE HUMAN ENDOGENOUS VIRUS HERV-K LONG TE RMINAL REPEAT IN AN INTRON OF THE ZNF91 GENE
    Bioorganiceskaa himia
    
    P.P. Khil et al., "THE HUMAN ENDOGENOUS VIRUS HERV-K LONG TE RMINAL REPEAT IN AN INTRON OF THE ZNF91 GENE", Bioorganiceskaa himia, 24(2), 1998, pp. 126-131
90. KHIL PP; LEBEDEV YB; SVERDLOV ED
    A NEW PUTATIVE GENE PREFERENTIALLY EXPRES SED IN THE HUMAN BRAIN LOCATED ON CHROMOSOME 19Q12 NEAR THE HUMAN ENDOGENOUS VIRUS HERV-K LTR
    Bioorganiceskaa himia
    
    P.P. Khil et al., "A NEW PUTATIVE GENE PREFERENTIALLY EXPRES SED IN THE HUMAN BRAIN LOCATED ON CHROMOSOME 19Q12 NEAR THE HUMAN ENDOGENOUS VIRUS HERV-K LTR", Bioorganiceskaa himia, 24(1), 1998, pp. 72-74
91. SUTO Y; ISHIKAWA Y; KASAHARA M; KASAI F; YABE T; AKAZA T; JUJI T
    GENE ARRANGEMENT OF THE KILLER-CELL INHIBITORY RECEPTOR FAMILY ON HUMAN-CHROMOSOME 19Q13.4 DETECTED BY FIBER FISH
    Immunogenetics (New York)
    
    Y. Suto et al., "GENE ARRANGEMENT OF THE KILLER-CELL INHIBITORY RECEPTOR FAMILY ON HUMAN-CHROMOSOME 19Q13.4 DETECTED BY FIBER FISH", Immunogenetics (New York), 48(4), 1998, pp. 235-241
92. GHAFFARI SR; BOYD E; CONNOR JM; JONES AM; TOLMIE JL
    MOSAIC SUPERNUMERARY RING CHROMOSOME-19 IDENTIFIED BY COMPARATIVE GENOMIC HYBRIDIZATION
    Journal of Medical Genetics
    
    S.R. Ghaffari et al., "MOSAIC SUPERNUMERARY RING CHROMOSOME-19 IDENTIFIED BY COMPARATIVE GENOMIC HYBRIDIZATION", Journal of Medical Genetics, 35(10), 1998, pp. 836-840
93. AKOPOV SB; NIKOLAEV LG; KHIL PP; LEBEDEV YB; SVERDLOV ED
    LONG TERMINAL REPEATS OF HUMAN ENDOGENOUS RETROVIRUS-K FAMILY (HERV-K) SPECIFICALLY BIND HOST-CELL NUCLEAR PROTEINS
    FEBS letters
    
    S.B. Akopov et al., "LONG TERMINAL REPEATS OF HUMAN ENDOGENOUS RETROVIRUS-K FAMILY (HERV-K) SPECIFICALLY BIND HOST-CELL NUCLEAR PROTEINS", FEBS letters, 421(3), 1998, pp. 229-233
94. GUSTAVSSON P; GARELLI E; DRAPTCHINSKAIA N; BALL S; WILLIG TN; TENTLER D; DIANZANI I; PUNNETT HH; SHAFER FE; CARIO H; RAMENGHI U; GLOMSTEIN A; PFEIFFER RA; GORINGE A; OLIVIERI NF; SMIBERT E; TCHERNIA G; ELINDER G; DAHL N
    IDENTIFICATION OF MICRODELETIONS SPANNING THE DIAMOND-BLACKFAN ANEMIALOCUS ON 19Q13 AND EVIDENCE FOR GENETIC-HETEROGENEITY
    American journal of human genetics
    
    P. Gustavsson et al., "IDENTIFICATION OF MICRODELETIONS SPANNING THE DIAMOND-BLACKFAN ANEMIALOCUS ON 19Q13 AND EVIDENCE FOR GENETIC-HETEROGENEITY", American journal of human genetics, 63(5), 1998, pp. 1388-1395
95. BRIGGS MD; MORTIER GR; COLE WG; KING LM; GOLIK SS; BONAVENTURE J; NUYTINCK L; DEPAEPE A; LEROY JG; BIESECKER L; LIPSON M; WILCOX WR; LACHMAN RS; RIMOIN DL; KNOWLTON RG; COHN DH
    DIVERSE MUTATIONS IN THE GENE FOR CARTILAGE OLIGOMERIC MATRIX PROTEININ THE PSEUDOACHONDROPLASIA MULTIPLE EPIPHYSEAL DYSPLASIA DISEASE SPECTRUM
    American journal of human genetics
    
    M.D. Briggs et al., "DIVERSE MUTATIONS IN THE GENE FOR CARTILAGE OLIGOMERIC MATRIX PROTEININ THE PSEUDOACHONDROPLASIA MULTIPLE EPIPHYSEAL DYSPLASIA DISEASE SPECTRUM", American journal of human genetics, 62(2), 1998, pp. 311-319
96. Canzian, F; Amati, P; Harach, HR; Kraimps, JL; Lesueur, F; Barbier, J; Levillain, P; Romeo, G; Bonneau, D
    A gene predisposing to familial thyroid tumors with cell oxyphilia maps tochromosome 19p13.2
    AMERICAN JOURNAL OF HUMAN GENETICS
    
    F. Canzian et al., "A gene predisposing to familial thyroid tumors with cell oxyphilia maps tochromosome 19p13.2", AM J HU GEN, 63(6), 1998, pp. 1743-1748
97. PALLAGI E; MOLNAR M; MOLNAR P; DIOSZEGHY P
    CENTRAL CORE AND NEMALINE RODS IN THE SAME PATIENT
    Acta Neuropathologica
    
    E. Pallagi et al., "CENTRAL CORE AND NEMALINE RODS IN THE SAME PATIENT", Acta Neuropathologica, 96(2), 1998, pp. 211-214
98. BELGE G; GARCIA E; RIPPE V; FUSCO A; BARTNITZKE S; BULLERDIEK J
    BREAKPOINTS OF 19Q13 TRANSLOCATIONS OF BENIGN THYROID-TUMORS MAP WITHIN A 400 KILOBASE REGION
    Genes, chromosomes & cancer
    
    G. Belge et al., "BREAKPOINTS OF 19Q13 TRANSLOCATIONS OF BENIGN THYROID-TUMORS MAP WITHIN A 400 KILOBASE REGION", Genes, chromosomes & cancer, 20(2), 1997, pp. 201-203
99. SULLIVAN AA; TEH BT; JEAVONS S; SCHALLING M; SILBURN P; LARSSON C; BOYLE R
    CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY
    Journal of clinical neuroscience
    
    A.A. Sullivan et al., "CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY", Journal of clinical neuroscience, 4(2), 1997, pp. 176-180
100. FENG GH; BAILIN T; OH J; SPRITZ RA
     MOUSE PALE EAR (EP) IS HOMOLOGOUS TO HUMAN HERMANSKY-PUDLAK-SYNDROME AND CONTAINS A RARE AT-AC INTRON
     Human molecular genetics
     
     G.H. Feng et al., "MOUSE PALE EAR (EP) IS HOMOLOGOUS TO HUMAN HERMANSKY-PUDLAK-SYNDROME AND CONTAINS A RARE AT-AC INTRON", Human molecular genetics, 6(5), 1997, pp. 793-797