Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where soggetti phrase all words 'CHROMOSOME-15' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 363 riferimenti
Si mostrano 100 riferimenti a partire da 1
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Turecki, G; Grof, P; Grof, E; D'Souza, V; Lebuis, L; Marineau, C; Cavazzoni, P; Duffy, A; Betard, C; Zvolsky, P; Robertson, C; Brewer, C; Hudson, TJ; Rouleau, GA; Alda, M
      Mapping susceptibility genes for bipolar disorder: a pharmacogenetic approach based on excellent response to lithium

      MOLECULAR PSYCHIATRY
    2. Runte, M; Farber, C; Lich, C; Zeschnigk, M; Buchholz, T; Smith, A; Van Maldergem, L; Burger, J; Muscatelli, F; Gillessen-Kaesbach, G; Horsthemke, B; Buiting, K
      Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15

      EUROPEAN JOURNAL OF HUMAN GENETICS
    3. Runte, M; Huttenhofer, A; Gross, S; Kiefmann, M; Horsthemke, B; Buiting, K
      The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

      HUMAN MOLECULAR GENETICS
    4. Rexroad, CE; Bennett, GL; Stone, RT; Keele, JW; Fahrenkrug, SC; Freking, BA; Kappes, SM; Smith, TPL
      Comparative mapping of BTA15 and HSA11 including a region containing a QTLfor meat tenderness

      MAMMALIAN GENOME
    5. Robic, A; Jeon, JT; Rey, V; Amarger, V; Chardon, P; Looft, C; Andersson, L; Gellin, J; Milan, D
      Construction of a high-resolution RH map of the human 2q35 region on TNG panel and comparison with a physical map of the porcine homologous region 15q25

      MAMMALIAN GENOME
    6. Moldavsky, M; Lev, D; Lerman-Sagie, T
      Behavioral phenotypes of genetic syndromes: A reference guide for psychiatrists

      JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
    7. Murdoch, JN; Rachel, RA; Shah, S; Beermann, F; Stanier, P; Mason, CA; Copp, AJ
      Circletail, a new mouse mutant with severe neural tube defects: Chromosomal localization and interaction with the loop-tail mutation

      GENOMICS
    8. Jeon, JT; Amarger, V; Rogel-Gaillard, C; Robic, A; Bongcam-Rudloff, E; Paul, S; Looft, C; Milan, D; Chardon, P; Andersson, L
      Comparative analysis of a BAC contig of the porcine RN region and the human transcript map: Implications for the cloning of trait loci

      GENOMICS
    9. Dorr, S; Midro, AT; Farber, C; Giannakudis, J; Hansmann, I
      Construction of a detailed physical and transcript map of the candidate region for Russell-Silver syndrome on chromosome 17q23-q24

      GENOMICS
    10. Prathikanti, S; McMahon, FJ
      Genome scans for susceptibility genes in bipolar affective disorder

      ANNALS OF MEDICINE
    11. Safioleas, MC; Kakisis, D; Evangelidakis, EL; Vericocos, CM; Manti, CP
      Thromboendarterectomy of the right common iliac artery in a patient with Marfan's syndrome and restoration with a new technique

      INTERNATIONAL ANGIOLOGY
    12. Motsouka, P; Samboni, C; Giannakoulas, N; Symeonidis, A; Zoumbos, N
      Polyploidy in acute promyelocytic leukemia without the 15 : 17 translocation

      HAEMATOLOGICA
    13. Balmer, D; LaSalle, JM
      Clonal maintenance of imprinted expression of SNRPN and IPW in normal lymphocytes: correlation with allele-specific methylation of SNRPN intron 1 butnot intron 7

      HUMAN GENETICS
    14. Lai, IC; Hong, CJ; Tsai, SJ
      Association study of a nicotinic receptor variant with schizophrenic disorders

      NEUROPSYCHOBIOLOGY
    15. Christison, KM; Schmutz, SM; Berryere, TG; Buchanan, FC
      Linkage mapping of MMP1 to cattle chromosome 15

      ANIMAL GENETICS
    16. Schlembach, D; Zenker, M; Trautmann, U; Ulmer, R; Beinder, E
      Deletion 15q24-26 in prenatally detected diaphragmatic hernia: increasing evidence of a candidate region for diaphragmatic development

      PRENATAL DIAGNOSIS
    17. Lee, MJ; Breese, CR; Strook, ML; Leonard, S
      The effect of nicotine and haloperidol co-treatment on nicotinic receptor levels in the rat brain

      MOLECULAR BRAIN RESEARCH
    18. Feusner, J; Ritchie, T; Lawford, B; Young, RM; Kann, B; Noble, EP
      GABA(A) receptor beta 3 subunit gene and psychiatric morbidity in a post-traumatic stress disorder population

      PSYCHIATRY RESEARCH
    19. Judge, DP; Biery, NJ; Dietz, HC
      Characterization of microsatellite markers flanking FBN1: Utility in the diagnostic evaluation for Marfan syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    20. Torrisi, L; Sangiorgi, E; Russo, L; Gurrieri, F
      Rearrangements of chromosome 15 in epilepsy

      AMERICAN JOURNAL OF MEDICAL GENETICS
    21. Tsuang, DW; Skol, AD; Faraone, SV; Bingham, S; Young, KA; Prabhudesai, S; Haverstock, SL; Mena, F; Menon, AS; Bisset, D; Pepple, J; Sauter, F; Baldwin, C; Weiss, D; Collins, J; Boehnke, M; Schellenberg, GD; Tsuang, MT
      Examination of genetic linkage of chromosome 15 to schizophrenia in a large veterans affairs cooperative study sample

      AMERICAN JOURNAL OF MEDICAL GENETICS
    22. Xu, JZ; Pato, MT; Dalla Torre, C; Medeiros, H; Carvalho, C; Basile, VS; Bauer, A; Dourado, A; Valente, J; Soares, MJ; Macedo, AA; Coelho, I; Ferreira, CP; Azevedo, MH; Macciardi, F; Kennedy, JL; Pato, CN
      Evidence for linkage disequilibrium between the alpha 7-nicotinic receptorgene (CHRNA7) locus and schizophrenia in Azorean families

      AMERICAN JOURNAL OF MEDICAL GENETICS
    23. Bolton, PF; Dennis, NR; Browne, CE; Thomas, NS; Veltman, MWM; Thompson, RJ; Jacobs, P
      The phenotypic manifestations of interstitial duplications of proximal 15qwith special reference to the autistic spectrum disorders

      AMERICAN JOURNAL OF MEDICAL GENETICS
    24. Freedman, R; Leonard, S; Olincy, A; Kaufmann, CA; Malaspina, D; Cloninger, CR; Svrakic, D; Faraone, SV; Tsuang, MT
      Evidence for the multigenic inheritance of schizophrenia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    25. Papadimitriou, GN; Dikeos, DG; Karadima, G; Avramopoulos, D; Daskalopoulou, EG; Stefanis, CN
      GABA-A receptor beta 3 and alpha 5 subunit gene cluster on chromosome 15q11-q13 and bipolar disorder: A genetic association study

      AMERICAN JOURNAL OF MEDICAL GENETICS
    26. Freedman, R; Leonard, S; Gault, JM; Hopkins, J; Cloninger, CR; Kaufmann, CA; Tsuang, MT; Farone, SV; Malaspina, D; Svrakic, DM; Sanders, A; Gejman, P
      Linkage disequilibrium for schizophrenia at the chromosome 15q13-14 locus of the alpha 7-nicotinic acetylcholine receptor subunit gene (CHRNA7)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    27. Akahoshi, K; Fukai, K; Kato, A; Kimiya, S; Kubota, T; Spritz, RA
      Duplication of 15q11.2-q14, including the P gene, in a woman with generalized skin hyperpigmentation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    28. Kato, R; Kishibayashi, J; Shimokawa, O; Harada, N; Niikawa, N; Matsumoto, N
      Congenital glaucoma and silver-russell phenotype associated with partial trisomy 7q and monosomy 15q

      AMERICAN JOURNAL OF MEDICAL GENETICS
    29. Tung, G; Covert, SM; Malabed, KL; Wohlferd, MM; Beckerman, KP; Goldberg, JD; Cotter, PD
      Minute supernumerary marker chromosomes identified in two patients with a related, larger pseudodicentric chromosome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    30. Santa Maria, LS; Curotto, B; Cortes, F; Rojas, C; Alliende, MA
      Methylation, cytogenetic and FISH tests in the molecular diagnosis of Prader-Willi and Angelman syndromes

      REVISTA MEDICA DE CHILE
    31. Gunay-Aygun, M; Schwartz, S; Heeger, S; O'Riordan, MA; Cassidy, SB
      The changing purpose of Prader-Willi syndrome clinical diagnostic criteriaand proposed revised criteria

      PEDIATRICS
    32. Tonnies, H; Schulze, I; Hennies, HC; Neumann, LM; Keitzer, R; Neitzel, H
      De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probes

      JOURNAL OF MEDICAL GENETICS
    33. Ungaro, P; Christian, SL; Fantes, JA; Mutirangura, A; Black, S; Reynolds, J; Malcolm, S; Dobyns, WB; Ledbetter, DH
      Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14

      JOURNAL OF MEDICAL GENETICS
    34. Amanna, IJ; Clise-Dwyer, K; Nashold, FE; Hoag, KA; Hayes, CE
      Cutting edge: A/WySnJ transitional B cells overexpress the chromosome 15 proapoptotic Blk gene and succumb to premature apoptosis

      JOURNAL OF IMMUNOLOGY
    35. Hanel, ML; Wevrick, R
      The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome

      CLINICAL GENETICS
    36. 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
    37. Corvin, A; O'Mahony, E; O'Regan, M; Comerford, C; O'Connell, R; Craddock, N; Gill, M
      Cigarette smoking and psychotic symptoms in bipolar affective disorder

      BRITISH JOURNAL OF PSYCHIATRY
    38. van Karnebeek, CDM; Naeff, MSJ; Mulder, BJM; Hennekam, RCM; Offringa, M
      Natural history of cardiovascular manifestations in Marfan syndrome

      ARCHIVES OF DISEASE IN CHILDHOOD
    39. Herzing, LBK; Kim, SJ; Cook, EH; Ledbetter, DH
      The human aminophospholipid-transporting ATPase gene ATP10C maps adjacent to UBE3A and exhibits similar imprinted expression

      AMERICAN JOURNAL OF HUMAN GENETICS
    40. Buiting, K; Barnicoat, A; Lich, C; Pembrey, M; Malcolm, S; Horsthemke, B
      Disruption of the bipartite imprinting center in a family with Angelman syndrome

      AMERICAN JOURNAL OF HUMAN GENETICS
    41. Allan, MF; Nielsen, MK; Pomp, D
      Gene expression in hypothalamus and brown adipose tissue of mice divergently selected for heat loss

      PHYSIOLOGICAL GENOMICS
    42. Ji, YG; Rebert, NA; Joslin, JM; Higgins, MJ; Schultz, RA; Nicholls, RD
      Structure of the highly conserved HERC2 gene and of multiple partially duplicated paralogs in human

      GENOME RESEARCH
    43. Mann, MRW; Bartolomei, MS
      Maintaining imprinting

      NATURE GENETICS
    44. Takeda, Y; Baba, A; Nakamura, F; Ito, M; Honma, H; Koyama, T
      Symptomatic generalized epilepsy associated with an inverted duplication of chromosome 15

      SEIZURE-EUROPEAN JOURNAL OF EPILEPSY
    45. Al Fadley, F; Al Manea, W; Nykanen, DG; Al Fadley, A; Bulbul, Z; Al Halees, Z
      Severe tortuosity and stenosis of the systemic, pulmonary and coronary vessels in 12 patients with similar phenotypic features: a new syndrome?

      CARDIOLOGY IN THE YOUNG
    46. Lee, SG; Cho, KA; Choi, YH; Montgomery, K; Lee, E; Miller, A; Kucherlapati, R; Song, K
      A sequence-ready map for human chromosome 12q15-21

      DNA SEQUENCE
    47. Looft, C; Milan, D; Jeon, JT; Paul, S; Reinsch, N; Rogel-Gaillard, C; Rey, V; Amarger, V; Robic, A; Kalm, E; Chardon, P; Andersson, L
      A high-density linkage map of the RN region in pigs

      GENETICS SELECTION EVOLUTION
    48. Maier, W; Schwab, S; Rietschel, M
      The genetics of schizophrenia

      CURRENT OPINION IN PSYCHIATRY
    49. Sundberg, JP; Boggess, D; Shultz, LD; Fijneman, RJA; Demant, P; Hogenesch, H; Cox, GA
      The chronic proliferative dermatitis mouse mutation (cpdm): mapping of themutant gene locus

      JOURNAL OF EXPERIMENTAL ANIMAL SCIENCE
    50. Horvat, S; Bunger, L; Falconer, VM; Mackay, P; Law, A; Bulfield, G; Keightley, PD
      Mapping of obesity QTLs in a cross between mouse lines divergently selected on fat content

      MAMMALIAN GENOME
    51. Freedman, R; Adams, CE; Leonard, S
      The alpha 7-nicotinic acetylcholine receptor and the pathology of hippocampal interneurons in schizophrenia

      JOURNAL OF CHEMICAL NEUROANATOMY
    52. Szeto, IYY; Li, LL; Surani, MA
      Ocat, a paternally expressed gene closely linked and transcribed in the opposite direction to Peg3

      GENOMICS
    53. Meadus, WJ; MacInnis, R
      Testing for the RN- gene in retail pork chops

      MEAT SCIENCE
    54. Walczak, C; Enders, H; Grissinger, K; Dufke, A
      Retrospective diagnosis of trisomy 15 in formalin-fixed, paraffin-embeddedplacental tissue in a newborn girl with Prader-Willi syndrome

      PRENATAL DIAGNOSIS
    55. Freedman, R; Adams, CE; Adler, LE; Bickford, PC; Gault, J; Harris, JG; Nagamoto, HT; Olincy, A; Ross, RG; Stevens, KE; Waldo, M; Leonard, S
      Inhibitory neurophysiological deficit as a phenotype for genetic investigation of schizophrenia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    56. Murphy, VE; Mynett-Johnson, LA; Claffey, E; Bergin, P; McAuliffe, M; Kealey, C; McKeon, P
      Search for bipolar disorder susceptibility loci: The application of a modified genome scan concentrating on gene-rich regions

      AMERICAN JOURNAL OF MEDICAL GENETICS
    57. Stassen, HH; Bridler, R; Hagele, S; Hergersberg, M; Mehmann, B; Schinzel, A; Weisbrod, M; Scharfetter, C
      Schizophrenia and smoking: Evidence for a common neurobiological basis?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    58. Riley, BP; Makoff, A; Mogudi-Carter, M; Jenkins, T; Williamson, R; Collier, D; Murray, R
      Haplotype transmission disequilibrium and evidence for linkage of the CHRNA7 gene region to schizophrenia in Southern African Bantu families

      AMERICAN JOURNAL OF MEDICAL GENETICS
    59. Durner, M; Shinnar, S; Resor, SR; Moshe, SL; Rosenbaum, D; Cohen, J; Harden, C; Kang, H; Hertz, S; Wallace, S; Luciano, D; Ballaban-Gil, K; Greenberg, DA
      No evidence for a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q

      AMERICAN JOURNAL OF MEDICAL GENETICS
    60. Tekin, M; Jackson-Cook, C; Buller, A; Ferreira-Gonzalez, A; Pandya, A; Garrett, CT; Bodurtha, J
      Fluorescence in situ hybridization detectable mosaicism for Angelman syndrome with biparental methylation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    61. Fridman, C; Koiffmann, CP
      Origin of uniparental disomy 15 in patients with Prader-Willi or Angelman syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    62. Rowe, AG; Abrams, L; Qu, Y; Chen, E; Cotter, PD
      Tetrasomy 15q25 -> qter: Cytogenetic and molecular characterization of an analphoid supernumerary marker chromosome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    63. Olander, E; Stamberg, J; Steinberg, L; Wulfsberg, EA
      Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with mosaic trisomy 15

      AMERICAN JOURNAL OF MEDICAL GENETICS
    64. Fridman, C; Varela, MC; Kok, F; Diament, A; Koiffmann, CP
      Paternal UPD15: Further genetic and clinical studies in four Angelman syndrome patients

      AMERICAN JOURNAL OF MEDICAL GENETICS
    65. Belleh, S; Zhou, GM; Wang, M; Der Kaloustian, VM; Pagon, RA; Godfrey, M
      Two novel fibrillin-2 mutations in congenital contractural arachnodactyly

      AMERICAN JOURNAL OF MEDICAL GENETICS
    66. Ming, JE; Blagowidow, N; Knoll, JHM; Rollings, L; Fortina, P; McDonald-McGinn, DM; Spinner, NB; Zackai, EH
      Submicroscopic deletion in cousins with Prader-Willi syndrome causes a grandmatrilineal inheritance pattern: Effects of imprinting

      AMERICAN JOURNAL OF MEDICAL GENETICS
    67. Milan, D; Jeon, JT; Looft, C; Amarger, V; Robic, A; Thelander, M; Rogel-Gaillard, C; Paul, S; Iannuccelli, N; Rask, L; Ronne, H; Lundstrom, K; Reinsch, N; Gellin, J; Kalm, E; Le Roy, P; Chardon, P; Andersson, L
      A mutation in PRKAG3 associated with excess glycogen content in pig skeletal muscle

      SCIENCE
    68. Lerch, N; Bosch, N; Muller, H; Malik, NJ
      Molecular genetic diagnosis of Prader-Willi and Angelman syndrome using a methylation-specific polymerase chain reaction

      MONATSSCHRIFT KINDERHEILKUNDE
    69. Nopola-Hemmi, J; Taipale, M; Haltia, T; Lehesjoki, AE; Voutilainen, A; Kere, J
      Two translocations of chromosome 15q associated with dyslexia

      JOURNAL OF MEDICAL GENETICS
    70. Miller, KD; Ellis, M; McKeith, FK; Bidner, BS; Meisinger, DJ
      Frequency of the rendement napole RN- allele in a population of American Hampshire pigs

      JOURNAL OF ANIMAL SCIENCE
    71. Leonard, S; Breese, C; Adams, C; Benhammou, K; Gault, J; Stevens, K; Lee, M; Adler, L; Olincy, A; Ross, R; Freedman, R
      Smoking and schizophrenia: abnormal nicotinic receptor expression

      EUROPEAN JOURNAL OF PHARMACOLOGY
    72. Cotter, PD; Ko, E; Larabell, SK; Rademaker, AW; Martin, RH
      Segregation of a supernumerary del(15) marker chromosome in sperm

      CLINICAL GENETICS
    73. McEntagart, ME; Webb, T; Hardy, C; King, MD
      Familial Prader-Willi syndrome: Case report and a literature review

      CLINICAL GENETICS
    74. Fridman, C; Santos, M; Ferrari, I; Koiffmann, CP
      A further Angelman syndrome patient with UPD15 due to paternal meiosis II nondisjunction

      CLINICAL GENETICS
    75. Sunahara, S; Nakamura, K; Nakao, K; Gondo, Y; Nagata, Y; Katsuki, M
      The oocyte-specific methylated region of the U2afbp-rs/U2af1-rs1 gene is dispensable for its imprinted methylation

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    76. Maziade, M; Merette, C; Cayer, M; Roy, MA; Szatmari, P; Cote, R; Thivierge, J
      Prolongation of brainstem auditory-evoked responses in autistic probands and their unaffected relatives

      ARCHIVES OF GENERAL PSYCHIATRY
    77. Zhao, HY; Li, JM; Robinson, WP
      Multipoint genetic mapping with uniparental disomy data

      AMERICAN JOURNAL OF HUMAN GENETICS
    78. Yoshihashi, H; Maeyama, K; Kosaki, R; Ogata, T; Tsukahara, M; Goto, Y; Hata, J; Matsuo, N; Smith, RJ; Kosaki, K
      Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome

      AMERICAN JOURNAL OF HUMAN GENETICS
    79. Rees, MI; Fenton, I; Williams, NM; Holmans, P; Norton, N; Cardno, A; Asherson, P; Spurlock, G; Roberts, E; Parfitt, E; Mant, P; Vallada, H; Dawson, E; Li, MW; Collier, DA; Powell, JF; Nanko, S; Gill, M; McGuffin, P; Owen, MJ
      Autosome search for schizophrenia susceptibility genes in multiply affected families

      MOLECULAR PSYCHIATRY
    80. McLeod, AG; Pai, M; Carter, RF; Squire, J; Barr, RD
      Familial evans syndrome: A report of an affected sibship

      JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    81. Smith, A
      The diagnosis of Prader-Willi syndrome

      JOURNAL OF PAEDIATRICS AND CHILD HEALTH
    82. Fisher, SE; Stein, JF; Monaco, AP
      A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia)

      EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
    83. Nothen, MM; Schulte-Korne, G; Grimm, T; Cichon, S; Vogt, IR; Muller-Myhsok, B; Propping, P; Remschmidt, H
      Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15

      EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
    84. Gillessen-Kaesbach, G; Demuth, S; Thiele, H; Theile, U; Lich, C; Horsthemke, B
      A previously unrecognised phenotype characterised by obesity, muscular hypotonia, and ability to speak in patients with Angelman syndrome caused by an imprinting defect

      EUROPEAN JOURNAL OF HUMAN GENETICS
    85. Moncla, A; Malzac, P; Voelckel, MA; Auquier, P; Girardot, L; Mattei, MG; Philip, N; Mattei, JF; Lalande, M; Livet, MO
      Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelmansyndrome patients

      EUROPEAN JOURNAL OF HUMAN GENETICS
    86. Farber, C; Dittrich, B; Buiting, K; Horsthemke, B
      The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletion

      HUMAN MOLECULAR GENETICS
    87. Koivisto, PA; Koivisto, H; Haapala, K; Simola, KOJ
      A de novo deletion of chromosome 15(q15.2q21.2) in a dysmorphic, mentally retarded child with congenital scalp defect

      CLINICAL DYSMORPHOLOGY
    88. Lorenzo, P; Aman, P; Sommarin, Y; Heinegard, D
      The human CILP gene: exon/intron organization and chromosomal mapping

      MATRIX BIOLOGY
    89. Southard-Smith, EM; Collins, JE; Ellison, JS; Smith, KJ; Baxevanis, AD; Touchman, JW; Green, ED; Dunham, I; Pavan, WJ
      Comparative analyses of the Dominant megacolon-SOX10 genomic interval in mouse and human

      MAMMALIAN GENOME
    90. Robic, A; Seroude, V; Jeon, JT; Yerle, M; Wasungu, L; Andersson, L; Gellin, J; Milan, D
      A radiation hybrid map of the RN region in pigs demonstrates conserved gene order compared with the human and mouse genomes

      MAMMALIAN GENOME
    91. Frankel, WN
      Detecting genes in new and old mouse models for epilepsy: a prospectus through the magnifying glass

      EPILEPSY RESEARCH
    92. Summers, JA; Feldman, MA
      Distinctive pattern of behavioral functioning in Angelman syndrome

      AMERICAN JOURNAL ON MENTAL RETARDATION
    93. Dykens, EM; Cassidy, SB; King, BH
      Maladaptive behavior differences in Prader-Willi syndrome due to paternal deletion versus maternal uniparental disomy

      AMERICAN JOURNAL ON MENTAL RETARDATION
    94. Bresters, D; Nikkels, PGJ; Meijboom, EJM; Hoorntje, TM; Pals, G; Beemer, FA
      Clinical, pathological and molecular genetic findings in a case of neonatal Marfan syndrome

      ACTA PAEDIATRICA
    95. Gutierrez, NC; Garcia, JL; Chillon, C; Muntion, S; Gonzalez, M; Hernandez, JM
      Cryptic insertion (15;17) in a case of acute promyelocytic leukemia detected by fluorescence in situ hybridization

      HAEMATOLOGICA
    96. Buoni, S; Grosso, S; Pucci, L; Fois, A
      Diagnosis of Angelman syndrome: clinical and EEG criteria

      BRAIN & DEVELOPMENT
    97. Laan, LAEM; van Haeringen, A; Brouwer, OF
      Angelman syndrome: a review of clinical and genetic aspects

      CLINICAL NEUROLOGY AND NEUROSURGERY
    98. Tuggle, CK; Sanchez-Serrano, I; Smith, B; Ernst, C; Marklund, L
      Cloning, sequencing and mapping the pig gene for the muscle-specific intermediate filament protein desmin (DES)

      ANIMAL GENETICS
    99. Cotter, PD; Ledesma, CT; Dietz, LG; Pusso, S; Wohlferd, MM; Goldberg, JD
      Prenatal diagnosis of supernumerary marker 15 chromosomes and exclusion ofuniparental disomy for chromosome 15

      PRENATAL DIAGNOSIS
    100. Salmon, B; Hallmayer, J; Rogers, T; Kalaydjieva, L; Petersen, PB; Nicholas, P; Pingree, C; McMahon, W; Spiker, D; Lotspeich, L; Kraemer, H; McCague, P; Dimiceli, S; Nouri, N; Pitts, T; Yang, J; Hinds, D; Myers, RM; Risch, N
      Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism

      AMERICAN JOURNAL OF MEDICAL GENETICS


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 27/10/20 alle ore 02:00:34