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Journal Abstract Search

207 related items for PubMed ID: 8958333

  • 21. Clinical and genetic studies on 12 preaxial polydactyly families and refinement of the localisation of the gene responsible to a 1.9 cM region on chromosome 7q36.
    Zguricas J, Heus H, Morales-Peralta E, Breedveld G, Kuyt B, Mumcu EF, Bakker W, Akarsu N, Kay SP, Hovius SE, Heredero-Baute L, Oostra BA, Heutink P.
    J Med Genet; 1999 Jan; 36(1):32-40. PubMed ID: 9950363
    [Abstract] [Full Text] [Related]

  • 22. A novel acropectoral syndrome maps to chromosome 7q36.
    Dundar M, Gordon TM, Ozyazgan I, Oguzkaya F, Ozkul Y, Cooke A, Wilkinson AG, Holloway S, Goodman FR, Tolmie JL.
    J Med Genet; 2001 May; 38(5):304-9. PubMed ID: 11333865
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  • 24. Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.
    Bruford EA, Riise R, Teague PW, Porter K, Thomson KL, Moore AT, Jay M, Warburg M, Schinzel A, Tommerup N, Tornqvist K, Rosenberg T, Patton M, Mansfield DC, Wright AF.
    Genomics; 1997 Apr 01; 41(1):93-9. PubMed ID: 9126487
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  • 25. Thumb/hallux duplication and preaxial polydactyly type I.
    Orioli IM, Castilla EE.
    Am J Med Genet; 1999 Jan 29; 82(3):219-24. PubMed ID: 10215544
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  • 26. A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10.
    Preston RA, Post JC, Keats BJ, Aston CE, Ferrell RE, Priest J, Nouri N, Losken HW, Morris CA, Hurtt MR.
    Nat Genet; 1994 Jun 29; 7(2):149-53. PubMed ID: 7920632
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  • 28. Postaxial polydactyly type A/B (PAP-A/B) is linked to chromosome 19p13.1-13.2 in a Chinese kindred.
    Zhao H, Tian Y, Breedveld G, Huang S, Zou Y, Y J, Chai J, Li H, Li M, Oostra BA, Lo WH, Heutink P.
    Eur J Hum Genet; 2002 Mar 29; 10(3):162-6. PubMed ID: 11973619
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  • 29. Phenotypic analysis of triphalangeal thumb and associated hand malformations.
    Zguricas J, Snijders PJ, Hovius SE, Heutink P, Oostra BA, Lindhout D.
    J Med Genet; 1994 Jun 29; 31(6):462-7. PubMed ID: 8071973
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  • 30. A new betaA1-crystallin splice junction mutation in autosomal dominant cataract.
    Bateman JB, Geyer DD, Flodman P, Johannes M, Sikela J, Walter N, Moreira AT, Clancy K, Spence MA.
    Invest Ophthalmol Vis Sci; 2000 Oct 29; 41(11):3278-85. PubMed ID: 11006214
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  • 32. Genetic linkage of autosomal dominant primary open angle glaucoma to chromosome 3q in a Greek pedigree.
    Kitsos G, Eiberg H, Economou-Petersen E, Wirtz MK, Kramer PL, Aspiotis M, Tommerup N, Petersen MB, Psilas K.
    Eur J Hum Genet; 2001 Jun 29; 9(6):452-7. PubMed ID: 11436127
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  • 33. The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes.
    McKay JD, Patterson B, Craig JE, Russell-Eggitt IM, Wirth MG, Burdon KP, Hewitt AW, Cohn AC, Kerdraon Y, Mackey DA.
    Br J Ophthalmol; 2005 Jul 29; 89(7):831-4. PubMed ID: 15965161
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  • 34. Linkage analysis with chromosome 9 markers in hereditary essential tremor.
    Conway D, Bain PG, Warner TT, Davis MB, Findley LJ, Thompson PD, Marsden CD, Harding AE.
    Mov Disord; 1993 Jul 29; 8(3):374-6. PubMed ID: 8341306
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  • 35. Evidence for clinical and genetic heterogeneity of syndactyly type I: the phenotype of second and third toe syndactyly maps to chromosome 3p21.31.
    Malik S, Schott J, Ali SW, Oeffner F, Amin-ud-Din M, Ahmad W, Grzeschik KH, Koch MC.
    Eur J Hum Genet; 2005 Dec 29; 13(12):1268-74. PubMed ID: 16189548
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  • 36. Evidence that a gene for essential tremor maps to chromosome 2p in four families.
    Higgins JJ, Loveless JM, Jankovic J, Patel PI.
    Mov Disord; 1998 Nov 29; 13(6):972-7. PubMed ID: 9827627
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  • 37. An autosomal dominant periodic fever associated with AA amyloidosis in a north Indian family maps to distal chromosome 1q.
    McDermott MF, Aganna E, Hitman GA, Ogunkolade BW, Booth DR, Hawkins PN.
    Arthritis Rheum; 2000 Sep 29; 43(9):2034-40. PubMed ID: 11014353
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  • 38. Triphalangeal thumb and psychomotor retardation: a new association?
    Rodriguez-Rojas LX, Macias NM, Barros-Nuñez P.
    Genet Couns; 2003 Sep 29; 14(1):39-43. PubMed ID: 12725588
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  • 39. Genetic analysis of syndactyly in German Holstein cattle.
    Drögemüller C, Distl O.
    Vet J; 2006 Jan 29; 171(1):120-5. PubMed ID: 16427589
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