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    1. Villar, AJ; Carlson, EJ; Gillespie, AM; Ursell, PC; Epstein, CJ
      Cardiomyopathy in mice with paternal uniparental disomy for chromosome 12

      GENESIS
    2. Trautner, MC; Sharief, N
      Pleural effusion in Noonan syndrome

      PRENATAL AND NEONATAL MEDICINE
    3. Degn, B; Lundorf, MD; Wang, A; Vang, M; Mors, O; Kruse, TA; Ewald, H
      Further evidence for a bipolar risk gene on chromosome 12q24 suggested by investigation of haplotype sharing and allelic association in patients fromthe Faroe Islands

      MOLECULAR PSYCHIATRY
    4. Charlier, C; Segers, K; Wagenaar, D; Karim, L; Berghams, S; Jaillon, O; Shay, T; Weissenbach, J; Cockett, N; Gyapay, G; Georges, M
      Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8

      GENOME RESEARCH
    5. Verpillat, P; Bouley, S; Campion, D; Hannequin, D; Dubois, B; Belliard, S; Puel, M; Thomas-Anterion, C; Agid, Y; Brice, A; Clerget-Darpoux, F
      Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population

      EUROPEAN JOURNAL OF HUMAN GENETICS
    6. Lawrance, LC; Fiocchi, C; Chakravarti, S
      Ulcerative colitis and Crohn's disease: distinctive gene expression profiles and navel susceptibility candidate genes

      HUMAN MOLECULAR GENETICS
    7. Verissimo, F; Jordan, P
      WNK kinases, a novel protein kinase subfamily in multi-cellular organisms

      ONCOGENE
    8. Rector, A; Vermeire, S; Thoelen, I; Keyaerts, E; Struyf, F; Vlietinck, R; Rutgeerts, P; Van Ranst, M
      Analysis of the CC chemokine receptor 5 (CCR5) delta-32 polymorphism in inflammatory bowel disease

      HUMAN GENETICS
    9. Cruts, M; Dermaut, B; Rademakers, R; Roks, G; Van den Broeck, M; Munteanu, G; van Duijn, CM; Van Broeckhoven, CV
      Amyloid beta secretase gene (BACE) is neither mutated in nor associated with early-onset Alzheimer's disease

      NEUROSCIENCE LETTERS
    10. Poduslo, SE; Yin, X
      Chromosome 12 and late-onset Alzheimer's disease

      NEUROSCIENCE LETTERS
    11. Ki, CS; Na, DL; Kim, HJ; Kim, JW
      Alpha-1 antichymotrypsin and alpha-2 macroglobulin gene polymorphisms are not associated with Korean late-onset Alzheimer's disease

      NEUROSCIENCE LETTERS
    12. Calogero, AE; De Palma, A; Grazioso, C; Barone, N; Burrello, N; Palermo, I; Gulisano, A; Pafumi, C; D'Agata, R
      High sperm aneuploidy rate in unselected infertile patients and its relationship with intracytoplasmic sperm injection outcome

      HUMAN REPRODUCTION
    13. Flaherty, MP; Grattan-Smith, P; Steinberg, A; Jamieson, R; Engle, EC
      Congenital fibrosis of the extraocular muscles associated with cortical dysplasia and maldevelopment of the basal ganglia

      OPHTHALMOLOGY
    14. Bertola, DR; Kim, CA; Pereira, AC; Mota, GFA; Krieger, JE; Vieira, IC; Valente, M; Loreto, MR; Magalhaes, RP; Gonzalez, CH
      Are Noonan syndrome and Noonan-like/multiple giant cell lesion syndrome distinct entities?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    15. McIlroy, SP; Dynan, KB; Vahidassr, DJ; Lawson, JT; Patterson, CC; Passmore, P
      Common polymorphisms in LRP and A2M do not affect genetic risk for Alzheimer disease in Northern Ireland

      AMERICAN JOURNAL OF MEDICAL GENETICS
    16. Rapley, EA; Hargrave, D; Persinguhe, N; Barfoot, R; Moore, I; Radford, M; Stratton, MR; Rahman, N; Pritchard-Jones, K
      Case of interstitial 12q deletion in association with Wilms tumor

      AMERICAN JOURNAL OF MEDICAL GENETICS
    17. Martin, DM; Gencyuz, CF; Petty, EM
      Systemic lupus erythematosus in a man with Noonan syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    18. Lendon, C; Craddock, N
      Is LBP-1c/CP2/LSF a disease-modifying gene for Alzheimer's disease?

      LANCET
    19. White, KE; Carn, G; Lorenz-Depiereux, B; Benet-Pages, A; Strom, TM; Econs, MJ
      Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23

      KIDNEY INTERNATIONAL
    20. Sorbi, S; Forleo, P; Tedde, A; Cellini, E; Ciantelli, M; Bagnoli, S; Nacmias, B
      Genetic risk factors in familial Alzheimer's disease

      MECHANISMS OF AGEING AND DEVELOPMENT
    21. Hiltunen, M; Mannermaa, A; Thompson, D; Easton, D; Pirskanen, M; Helisalmi, S; Koivisto, AM; Lehtovirta, M; Ryynanen, M; Soininen, H
      Genome-wide linkage disequilibrium mapping of late-onset Alzheimer's disease in Finland

      NEUROLOGY
    22. Mariani, R; Rasala, BA; Rutter, G; Wiegers, K; Brandt, SM; Krausslich, HG; Landau, NR
      Mouse-human heterokaryons support efficient human immunodeficiency virus type 1 assembly

      JOURNAL OF VIROLOGY
    23. Jhoo, JH; Kim, KW; Lee, DY; Lee, KU; Lee, JH; Kim, SY; Youn, JY; Youn, JC; Woo, JI
      Association of alpha-2-macroglobulin deletion polymorphism with sporadic Alzheimer's disease in Koreans

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    24. Shivaram, SM; Engle, EC; Petersen, RA; Robb, RM
      Congenital fibrosis syndromes

      INTERNATIONAL OPHTHALMOLOGY CLINICS
    25. Williams, KL; Nanda, I; Lyons, GE; Kuo, CT; Schmid, M; Leiden, JM; Kaplan, MH; Taparowsky, EJ
      Characterization of murine BATF: a negative regulator of activator protein-1 activity in the thymus

      EUROPEAN JOURNAL OF IMMUNOLOGY
    26. Craddock, N; Jones, I
      Molecular genetics of bipolar disorder

      BRITISH JOURNAL OF PSYCHIATRY
    27. Clark, AJL; Metherell, L; Swords, FM; Elias, LLK
      The molecular pathogenesis of ACTH insensitivity syndromes

      ANNALES D ENDOCRINOLOGIE
    28. van Heel, DA; Jewell, DP
      Genetics of inflammatory bowel disease - an update

      ACTA GASTRO-ENTEROLOGICA BELGICA
    29. Bertram, L; Blacker, D; Crystal, AS; Jones, J; Keeney, D; MacKenzie-Ingano, L; Mullin, K; Basu, S; Yhu, S; McInnis, M; Go, RCP; Saunders, AJ; Tanzi, RE
      Candidate genes showing no evidence of association with Alzheimer's disease: Results of the NIMH-AD genetics initiative

      ALZHEIMER'S DISEASE
    30. Seki, N; Ueki, N; Yano, K; Saito, T; Masuho, Y; Muramatsu, M
      cDNA cloning of a novel human gene NAKAP95, neighbor of A-kinase anchoringprotein 95 (AKAP95) on chromosome 19p13.11-p13.12 region

      JOURNAL OF HUMAN GENETICS
    31. Justesen, J; Hartmann, R; Kjeldgaard, NO
      Gene structure and function of the 2 '-5 '-oligoadenylate synthetase family

      CELLULAR AND MOLECULAR LIFE SCIENCES
    32. Shirley, MW; Harvey, DA
      A genetic linkage map of the apicomplexan protozoan parasite Eimeria tenella

      GENOME RESEARCH
    33. Stokkers, PCF; Huibregtse, K; Leegwater, AC; Reitsma, PH; Tytgat, GNJ; van Deventer, SJH
      Analysis of a positional candidate gene for inflammatory bowel disease: NRAMP2

      INFLAMMATORY BOWEL DISEASES
    34. Zhang, WJ; Koltun, WA; Tilberg, AF; Page, MJ; Chorney, TJ
      Absence of GNAI2 codon 179 oncogene mutations in inflammatory bowel disease

      INFLAMMATORY BOWEL DISEASES
    35. Pellegata, NS; Dieguez-Lucena, JL; Joensuu, T; Lau, S; Montgomery, KT; Krahe, R; Kivela, T; Kucherlapati, R; Forsius, H; de la Chapelle, A
      Mutations in KERA, encoding keratocan, cause cornea plana

      NATURE GENETICS
    36. Zhao, S; Li, K; Yu, M; Peng, Z
      Ordering three microsatellites on porcine chromosome 12 by single sperm typing

      ANIMAL BIOTECHNOLOGY
    37. Hadj-Rabia, S; Salomon, R; Pelet, A; Penet, C; Rotschild, A; de Laet, MH; Chaouachi, B; Hannachi, R; Bakiri, F; Brauner, R; Chaussain, JL; Munnich, A; Lyonnet, S
      Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    38. Berg, J; Grace, E; Teik, KW; Hammond, H; Tidman, M; FitzPatrick, D
      Bullous ichthyosiform erythroderma, developmental delay, aortic and pulmonary stenosis in association with a FRA12A

      CLINICAL DYSMORPHOLOGY
    39. Georgiades, P; Watkins, M; Surani, MA; Ferguson-Smith, AC
      Parental origin-specific developmental defects in mice with uniparental disomy for chromosome 12

      DEVELOPMENT
    40. Issa, AM; Keyserlingk, EW
      Apolipoprotein E genotyping for pharmacogenetic purposes in Alzheimer's disease: Emerging ethical issues

      CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE
    41. Zhao, YG; Hermesz, E; Yarolin, MC; Westphal, H
      Genomic structure, chromosomal localization and expression of the human LIM-homeobox gene LHX5

      GENE
    42. White, KE; Lorenz, B; Evans, WE; Meitinger, T; Strom, TM; Econs, MJ
      Molecular cloning of a novel human UDP-GalNAc : polypeptide N-acetylgalactosaminyltransferase, GalNAc-T8, and analysis as a candidate autosomal dominant hypophosphatemic rickets (ADHR) gene

      GENE
    43. Numakura, C; Lin, CQ; Oka, N; Akiguchi, I; Hayasaka, K
      Hemizygous mutation of the peripheral myelin protein 22 gene associated with Charcot-Marie-Tooth disease type 1

      ANNALS OF NEUROLOGY
    44. Romas, SN; Mayeux, R; Rabinowitz, D; Tang, MX; Zadroga, HR; Lantigua, R; Medrano, M; Tycko, B; Knowles, JA
      The deletion polymorphism and Val1000lle in alpha-2-macroglobulin and Alzheimer disease in Caribbean Hispanics

      NEUROSCIENCE LETTERS
    45. Bottini, N; Gloria-Bottini, F; Lucarini, N; Ronchetti, PG; Fontana, L
      Inflammatory bowel disease: Are there gender differences in the genetics of signal transduction? A preliminary study of cytosolic low molecular weight protein tyrosine phosphatase

      DISEASE MARKERS
    46. Araki, T; Milbrandt, J
      Ninjurin2, a novel homophilic adhesion molecule, is expressed in mature sensory and enteric neurons and promotes neurite outgrowth

      JOURNAL OF NEUROSCIENCE
    47. Schmutz, SM; Berryere, TG; Buchanan, FC
      An SNP in DCT is used for linkage mapping on cattle chromosome 12

      ANIMAL GENETICS
    48. Dalwadi, H; Bo, W; Braun, J
      Defining new pathogens and nonculturable infectious agents associated withinflammatory bowel disease

      CURRENT OPINION IN GASTROENTEROLOGY
    49. Blank, C; Rogalla, P; Tran, KH; Bullerdiek, J
      A novel high mobility group protein gene is a candidate for Xp22 abnormalities in uterine leiomyomas and other benign tumors

      CANCER GENETICS AND CYTOGENETICS
    50. Scantamburlo, G; Lampertz, S; Croisiau, C; Jamar, M; Koulischer, L; Herens, C
      Inv(12)(q15q24): A nonrandom change associated with myelodysplasia?

      CANCER GENETICS AND CYTOGENETICS
    51. Shadan, FF; Mascarello, JT; Newbury, RO; Dennis, T; Spallone, P; Stock, AD
      Supernumerary ring chromosomes derived from the long arm of chromosome 12 as the primary cytogenetic anomaly in a rare soft tissue chondroma

      CANCER GENETICS AND CYTOGENETICS
    52. DeLozier-Blanchet, CD; Roeder, E; Denis-Arrue, R; Blouin, JL; Low, J; Fisher, J; Scharnhorst, D; Curry, CJ
      Trisomy 12 mosaicism confirmed in multiple organs from a liveborn child

      AMERICAN JOURNAL OF MEDICAL GENETICS
    53. Rauen, KA; Cotter, PD; Bitts, SR; Cox, VA; Golabi, M
      Cardio-facio-cutaneous syndrome phenotype in an individual with an interstitial deletion of 12q: Identification of a candidate region for CFC syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    54. Vesaluoma, MH; Sankila, EM; Gallar, J; Muller, LJ; Petroll, WM; Moilanen, JAO; Forsius, H; Tervo, TMT
      Autosomal recessive cornea plana: In vivo corneal morphology and corneal sensitivity

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    55. Koster, MN; Dermaut, B; Cruts, M; Houwing-Duistermaat, JJ; Roks, G; Tol, J; Ott, A; Hofman, A; Munteanu, G; Breteler, MMB; van Duijn, CM; Van Broeckhoven, C
      The alpha 2-macroglobulin gene in AD - A population-based study and meta-analysis

      NEUROLOGY
    56. Mrissa, N; Belal, S; Ben Hamida, C; Amouri, R; Turki, I; Mrissa, R; Ben Hamida, M; Hentati, F
      Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxiain a Tunisian family

      NEUROLOGY
    57. Gibson, AM; Singleton, AB; Smith, G; Woodward, R; McKeith, IG; Perry, RH; Ince, PG; Ballard, CG; Edwardson, JA; Morris, CM
      Lack of association of the alpha 2-macroglobulin locus on chromosome 12 inAD

      NEUROLOGY
    58. Dumoutier, L; Van Roost, E; Colau, D; Renauld, JC
      Human interleukin-10-related T cell-derived inducible factor: Molecular cloning and functional characterization as an hepatocyte-stimulating factor

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    59. Mariani, R; Rutter, G; Harris, ME; Hope, TJ; Krausslich, HG; Landau, NR
      A block to human immunodeficiency virus type 1 assembly in murine cells

      JOURNAL OF VIROLOGY
    60. Bieniasz, PD; Cullen, BR
      Multiple blocks to human immunodeficiency virus type 1 replication in rodent cells

      JOURNAL OF VIROLOGY
    61. Ion, A; Crosby, AH; Kremer, H; Kenmochi, N; Van Reen, M; Fenske, C; Van der Burgt, I; Brunner, HG; Montgomery, K; Kucherlapati, RS; Patton, MA; Page, DC; Mariman, E; Jeffery, S
      Detailed mapping, mutation analysis, and intragenic polymorphism identification in candidate Noonan syndrome genes MYL2, DCN, EPS8, and RPL6

      JOURNAL OF MEDICAL GENETICS
    62. Newman, G; Crooke, E
      DnaA, the initiator of Escherichia coli chromosomal replication, is located at the cell membrane

      JOURNAL OF BACTERIOLOGY
    63. Lesage, S; Zouali, H; Colombel, JF; Belaiche, J; Cezard, JP; Tysk, C; Almer, S; Gassull, M; Binder, V; Chamaillard, M; Le Gall, I; Thomas, G; Hugot, JP
      Genetic analyses of chromosome 12 loci in Crohn's disease

      GUT
    64. Simmons, JD; Mullighan, C; Welsh, KI; Jewell, DP
      Vitamin D receptor gene polymorphism: association with Crohn's disease susceptibility

      GUT
    65. Glass, IA; Trenholme, A; Mildenhall, L; Bailey, RJ; Cotter, PD
      Mild phenotype in two siblings with distal monosomy 12p13.31 -> pter

      CLINICAL GENETICS
    66. Lasso, JM; Espana, A; Zudaire, MI; De Alava, E; Bazan, A
      Congenital infiltrating lipoma of the upper limb in a patient with von Willebrand disease

      BRITISH JOURNAL OF DERMATOLOGY
    67. Esipova, NG; Kutuzova, GI; Makeev, VY; Frank, GK; Balandina, AV; Kamashev, DE; Karpov, VL
      Analysis of peculiarities in nucleotides disposition in the origin of chromosome replication-oriC from Escherichia coli

      BIOFIZIKA
    68. Traboulsi, EI; Lee, BA; Mousawi, A; Khamis, AR; Engle, EC
      Evidence of genetic heterogeneity in autosomal recessive congenital fibrosis of the extraocular muscles

      AMERICAN JOURNAL OF OPHTHALMOLOGY
    69. Lake, SL; Blacker, D; Laird, NM
      Family-based tests of association in the presence of linkage

      AMERICAN JOURNAL OF HUMAN GENETICS
    70. Chena, C; Sarmiento, M; Palacios, MF; Scolnik, M; Slavutsky, I
      dup(12)(q13-q22) and 13q14 deletion in a case of B-cell chronic lymphocytic leukemia

      ACTA HAEMATOLOGICA
    71. Mokliatchouk, O; Blacker, D; Rabinowitz, D
      Association tests for traits with variable age at onset

      HUMAN HEREDITY
    72. Yang, HY; Ohmen, JD; Ma, YH; Targan, SR; Fischel-Ghodsian, N; Rotter, JI
      Additional evidence of linkage between Crohn's disease and a putative locus on chromosome 12

      GENETICS IN MEDICINE
    73. Murty, VVVS; Montgomery, K; Dutta, S; Bala, S; Renault, B; Bosl, GJ; Kucherlapati, R; Chaganti, RSK
      A 3-Mb high-resolution BAC/PAC contig of 12q22 encompassing the 830-kb consensus minimal deletion in male germ cell tumors

      GENOME RESEARCH
    74. Bisogno, G; Murgia, A; Mammi, I; Strafella, MS; Carli, M
      Rhabdomyosarcoma in a patient with cardio-facio-cutaneous syndrome

      JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    75. Rogaeva, EA; Premkumar, S; Grubber, J; Serneels, L; Scott, WK; Kawarai, T; Song, YQ; Hill, DM; Abou-Donia, SM; Martin, ER; Vance, JJ; Yu, G; Orlacchio, A; Pei, Y; Nishimura, M; Supala, A; Roberge, B; Saunders, AM; Roses, AD; Schmechel, D; Crane-Gatherum, A; Sorbi, S; Bruni, A; Small, GW; Conneally, PM; Haines, JL; Van Leuven, F; St George-Hyslop, PH; Farrer, LA; Pericak-Vance, MA
      An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease

      NATURE GENETICS
    76. Kelsell, DP; Stevens, HP; Purkis, PE; Talas, U; Rustin, MHA; Leigh, IM
      Fine genetic mapping of diffuse non-epidermolytic palmoplantar keratodermato chromosome 12q11-q13: exclusion of the mapped type II keratins

      EXPERIMENTAL DERMATOLOGY
    77. Taymans, SE; Pack, S; Pak, E; Orban, Z; Barsony, J; Zhuang, ZP; Stratakis, CA
      The human vitamin D receptor gene (VDR) is localized to region 12cen-q12 by fluorescent in situ hybridization and radiation hybrid mapping: Genetic and physical VDR map

      JOURNAL OF BONE AND MINERAL RESEARCH
    78. Engle, E
      A genetic approach to congenital extraocular muscle disorders

      JOURNAL OF CHILD NEUROLOGY
    79. Aissani, B; Sinnett, D
      Fine physical and transcript mapping of a 1.8 Mb region spanning the locusfor childhood acute lymphoblastic leukemia on chromosome 12p12.3

      GENE
    80. Myllykangas, L; Polvikoski, T; Sulkava, R; Verkkoniemi, A; Crook, R; Tienari, PJ; Pusa, AK; Niinisto, L; O'Brien, P; Kontula, K; Hardy, J; Haltia, M; Perez-Tur, J
      Genetic association of alpha(2)-macroglobulin with Alzheimer's disease in a Finnish elderly population

      ANNALS OF NEUROLOGY
    81. Ragazzini, P; Gamberi, G; Benassi, MS; Orlando, C; Sestini, R; Ferrari, C; Molendini, L; Sollazzo, MR; Merli, M; Magagnoli, G; Bertoni, F; Bohling, T; Pazzagli, M; Picci, P
      Analysis of SAS gene and CDK4 and MDM2 proteins in low-grade osteosarcoma

      CANCER DETECTION AND PREVENTION
    82. Wavrant-DeVrieze, F; Lambert, JC; Stas, L; Crook, R; Cottel, D; Pasquier, F; Frigard, B; Lambrechts, M; Thiry, E; Amouyel, P; Tur, JP; Chartier-Harlin, MC; Hardy, J; Van Leuven, F
      Association between coding variability in the LRP gene and the risk of late-onset Alzheimer's disease

      HUMAN GENETICS
    83. Huebner, A; Elias, LLK; Clark, AJL
      ACTH resistance syndromes

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    84. Korovaitseva, GI; Premkumar, S; Grigorenko, A; Molyaka, Y; Galimbet, V; Selezneva, N; Gavrilova, SI; Farrer, LA; Rogaev, EI
      Alpha-2 macroglobulin gene in early- and late-onset Alzheimer disease

      NEUROSCIENCE LETTERS
    85. Crawford, F; Town, T; Freeman, M; Schinka, J; Gold, M; Duara, R; Mullan, M
      The alpha-2 macroglobulin gene is not associated with Alzheimer's disease in a case-control sample

      NEUROSCIENCE LETTERS
    86. Beffert, U; Arguin, C; Poirier, J
      The polymorphism in exon 3 of the low density lipoprotein receptor-relatedprotein gene is weakly associated with Alzheimer's disease

      NEUROSCIENCE LETTERS
    87. St George-Hyslop, PH
      Molecular genetics of Alzheimer Disease

      SEMINARS IN NEUROLOGY
    88. Napolitano, G; Licciardo, P; Gallo, P; Majello, B; Giordano, A; Lania, L
      The CDK9-associated cyclins T1 and T2 exert opposite effects on HIV-1 Tat activity

      AIDS
    89. Sun, HS; Yerle, M; Pinton, P; Chardon, P; Rogel-Gaillard, C; Lyons, LA; Laughlin, TF; Tuggle, CK
      Physical assignments of human chromosome 13 genes on pig chromosome 11 demonstrate extensive synteny and gene order conservation between pig and human

      ANIMAL GENETICS
    90. Nisbet, DL; Griffin, DR; Chitty, LS
      Prenatal features of Noonan syndrome

      PRENATAL DIAGNOSIS
    91. El-Naggar, AK; Lovell, M; Callender, DL; Ordonez, NG; Killary, AM
      Cytogenetic analysis of a primary salivary gland myoepithelioma

      CANCER GENETICS AND CYTOGENETICS
    92. Goi, K; Sugita, K; Nakamura, M; Miyamoto, N; Karakida, N; Iijima, K; Nakazawa, S
      Development of acute lymphoblastic leukemia with translocation (4;11) in ayoung girl with familial pericentric inversion 12

      CANCER GENETICS AND CYTOGENETICS
    93. Smolarek, TA; Blough, RI; Foster, RS; Ulbright, TM; Palmer, CG; Heerema, NA
      Cytogenetic analyses of 85 testicular germ cell tumors: Comparison of postchemotherapy and untreated tumors

      CANCER GENETICS AND CYTOGENETICS
    94. Town, T; Paris, D; Parker, TA; Kundtz, A; Tan, J; Duara, R; Gold, M; Crawford, F; Mullan, M
      Alzheimers disease is not associated with the hypertension genetic risk factors PLA(2) or G protein beta 3, either independently or interactively with apolipoprotein E

      AMERICAN JOURNAL OF MEDICAL GENETICS
    95. Franks, E; Guy, C; Jacobsen, N; Bowen, T; Owen, MJ; O'Donovan, MC; Craddock, N
      Eleven trinucleotide repeat loci that map to chromosome 12 excluded from involvement in the pathogenesis of bipolar disorder

      AMERICAN JOURNAL OF MEDICAL GENETICS
    96. Viggiano, L; Miolla, V; Ricco, A; Storlazzi, CT; Pennacchia, M; Fratello, A; Mancini, M; Marzella, R; Archidiacono, N; Rocchi, M
      Molecular cytogenetic resources specific for chromosome 12

      AMERICAN JOURNAL OF MEDICAL GENETICS
    97. Sathya, P; Tomkins, DJ; Freeman, V; Paes, B; Nowaczyk, JM
      De novo deletion 12q: Report of a patient with 12q24.31q24.33 deletion

      AMERICAN JOURNAL OF MEDICAL GENETICS
    98. Doherty, EJ; Macy, ME; Wang, SM; Dykeman, CP; Melanson, MT; Engle, EC
      CFEOM3: A new extraocular congenital fibrosis syndrome that maps to 16q24.2-q24.3

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    99. Barten, R; Trowsdale, J
      The human Ly-49L gene

      IMMUNOGENETICS
    100. Kuan, AP; Chamberlain, W; Malkiel, S; Lieu, HD; Factor, SM; Diamond, B; Kotzin, BL
      Genetic control of autoimmune myocarditis mediated by myosin-specific antibodies

      IMMUNOGENETICS


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Documento generato il 20/02/20 alle ore 00:03:17