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    Results: 1 to 20 of 192

    1.

    A novel gene for neonatal diabetes maps to chromosome 10p12.1-p13.

    Sellick GS, Garrett C, Houlston RS.

    Diabetes. 2003 Oct;52(10):2636-8.PMID: 14514650 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Genomewide linkage searches for Mendelian disease loci can be efficiently conducted using high-density SNP genotyping arrays.

    Sellick GS, Longman C, Tolmie J, Newbury-Ecob R, Geenhalgh L, Hughes S, Whiteford M, Garrett C, Houlston RS.

    Nucleic Acids Res. 2004 Nov 23;32(20):e164.PMID: 15561999 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.

    Mustapha M, Chouery E, Chardenoux S, Naboulsi M, Paronnaud J, Lemainque A, Mégarbané A, Loiselet J, Weil D, Lathrop M, Petit C.

    Eur J Hum Genet. 2002 Mar;10(3):210-2.PMID: 11973626 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Genomewide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome 5q14.3-q21.1.

    Tang YG, Rabinowitz YS, Taylor KD, Li X, Hu M, Picornell Y, Yang H.

    Genet Med. 2005 Jul-Aug;7(6):397-405.PMID: 16024971 [PubMed - indexed for MEDLINE]Related articles

    5.

    Mapping of hereditary mixed polyposis syndrome (HMPS) to chromosome 10q23 by genomewide high-density single nucleotide polymorphism (SNP) scan and identification of BMPR1A loss of function.

    Cao X, Eu KW, Kumarasinghe MP, Li HH, Loi C, Cheah PY.

    J Med Genet. 2006 Mar;43(3):e13.PMID: 16525031 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    A new locus for autosomal recessive non-syndromic mental retardation maps to 1p21.1-p13.3.

    Uyguner O, Kayserili H, Li Y, Karaman B, Nürnberg G, Hennies H, Becker C, Nürnberg P, Başaran S, Apak MY, Wollnik B.

    Clin Genet. 2007 Mar;71(3):212-9.PMID: 17309643 [PubMed - indexed for MEDLINE]Related articles

    7.

    A novel genetic study of Chinese families with autosomal recessive retinitis pigmentosa.

    Abd El-Aziz MM, El-Ashry MF, Chan WM, Chong KL, Barragan I, Antiñolo G, Pang CP, Bhattacharya SS.

    Ann Hum Genet. 2007 May;71(Pt 3):281-94. Epub 2006 Nov 29.PMID: 17156103 [PubMed - indexed for MEDLINE]Related articles

    8.

    Identification of multiple loci for Alzheimer disease in a consanguineous Israeli-Arab community.

    Farrer LA, Bowirrat A, Friedland RP, Waraska K, Korczyn AD, Baldwin CT.

    Hum Mol Genet. 2003 Feb 15;12(4):415-22.PMID: 12566388 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    A gene causing autosomal recessive cataract maps to the short arm of chromosome 3.

    Pras E, Pras E, Bakhan T, Levy-Nissenbaum E, Lahat H, Assia EI, Garzozi HJ, Kastner DL, Goldman B, Frydman M.

    Isr Med Assoc J. 2001 Aug;3(8):559-62.PMID: 11519376 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13.

    Teltsh O, Kanyas K, Karni O, Levi A, Korner M, Ben-Asher E, Lancet D, Hamdan A, Lerer B, Kohn Y.

    Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):209-15.PMID: 17823922 [PubMed - indexed for MEDLINE]Related articles

    11.

    Mutations in PTF1A cause pancreatic and cerebellar agenesis.

    Sellick GS, Barker KT, Stolte-Dijkstra I, Fleischmann C, Coleman RJ, Garrett C, Gloyn AL, Edghill EL, Hattersley AT, Wellauer PK, Goodwin G, Houlston RS.

    Nat Genet. 2004 Dec;36(12):1301-5. Epub 2004 Nov 14.PMID: 15543146 [PubMed - indexed for MEDLINE]Related articles

    12.

    Maturity onset diabetes of the young is not linked to the insulin gene.

    Bell JI, Wainscoat JS, Old JM, Chlouverakis C, Keen H, Turner RC, Weatherall DJ.

    Br Med J (Clin Res Ed). 1983 Feb 19;286(6365):590-2.PMID: 6402160 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    Assessment of the role of common genetic variation in the transient neonatal diabetes mellitus (TNDM) region in type 2 diabetes: a comparative genomic and tagging single nucleotide polymorphism approach.

    Gloyn AL, Mackay DJ, Weedon MN, McCarthy MI, Walker M, Hitman G, Knight BA, Owen KR, Hattersley AT, Frayling TM.

    Diabetes. 2006 Aug;55(8):2272-6.PMID: 16873690 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    A genome-wide search for risk genes using homozygosity mapping and microarrays with 1,494 single-nucleotide polymorphisms in 22 eastern Cuban families with bipolar disorder.

    Ewald H, Wikman FP, Teruel BM, Buttenschön HN, Torralba M, Als TD, El Daoud A, Flint TJ, Jorgensen TH, Blanco L, Kruse TA, Orntoft TF, Mors O.

    Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):25-30.PMID: 15558715 [PubMed - indexed for MEDLINE]Related articles

    15.

    Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness.

    Lezirovitz K, Pardono E, de Mello Auricchio MT, de Carvalho E Silva FL, Lopes JJ, Abreu-Silva RS, Romanos J, Batissoco AC, Mingroni-Netto RC.

    Eur J Hum Genet. 2008 Jan;16(1):89-96. Epub 2007 Sep 12. Erratum in: Eur J Hum Genet. 2008 May;16(5):660. PMID: 17851452 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci.

    Burdon KP, Coster DJ, Charlesworth JC, Mills RA, Laurie KJ, Giunta C, Hewitt AW, Latimer P, Craig JE.

    Hum Genet. 2008 Nov;124(4):379-86. Epub 2008 Sep 5.PMID: 18795334 [PubMed - indexed for MEDLINE]Related articles

    17.

    A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3.

    Aslam M, Wajid M, Chahrour MH, Ansar M, Haque S, Pham TL, Santos RP, Yan K, Ahmad W, Leal SM.

    Am J Med Genet A. 2005 Feb 15;133A(1):18-22.PMID: 15641023 [PubMed - indexed for MEDLINE]Related articles

    18.

    GAD2 on chromosome 10p12 is a candidate gene for human obesity.

    Boutin P, Dina C, Vasseur F, Dubois S, Corset L, Séron K, Bekris L, Cabellon J, Neve B, Vasseur-Delannoy V, Chikri M, Charles MA, Clement K, Lernmark A, Froguel P.

    PLoS Biol. 2003 Dec;1(3):E68. Epub 2003 Nov 3.PMID: 14691540 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    A gene for Leber's congenital amaurosis maps to chromosome 17p.

    Camuzat A, Dollfus H, Rozet JM, Gerber S, Bonneau D, Bonnemaison M, Briard ML, Dufier JL, Ghazi I, Leowski C, et al.

    Hum Mol Genet. 1995 Aug;4(8):1447-52.PMID: 7581387 [PubMed - indexed for MEDLINE]Related articles

    20.

    Genome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathy.

    Oberti C, Wang L, Li L, Dong J, Rao S, Du W, Wang Q.

    Circulation. 2004 Dec 21;110(25):3753-9. Epub 2004 Dec 13.PMID: 15596564 [PubMed - indexed for MEDLINE]Related articlesFree article

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