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Journal Abstract Search

238 related items for PubMed ID: 9950363

  • 1. 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
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  • 3. Homozygous feature of isolated triphalangeal thumb-preaxial polydactyly linked to 7q36: no phenotypic difference between homozygotes and heterozygotes.
    Semerci CN, Demirkan F, Ozdemir M, Biskin E, Akin B, Bagci H, Akarsu NA.
    Clin Genet; 2009 Jul; 76(1):85-90. PubMed ID: 19519794
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  • 4. 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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  • 5. An autosomal dominant triphalangeal thumb: polysyndactyly syndrome with variable expression in a large Indian family maps to 7q36.
    Radhakrishna U, Blouin JL, Solanki JV, Dhoriani GM, Antonarakis SE.
    Am J Med Genet; 1996 Dec 11; 66(2):209-15. PubMed ID: 8958333
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  • 9. A 300-kb microduplication of 7q36.3 in a patient with triphalangeal thumb-polysyndactyly syndrome combined with congenital heart disease and optic disc coloboma: a case report.
    Zlotina A, Melnik O, Fomicheva Y, Skitchenko R, Sergushichev A, Shagimardanova E, Gusev O, Gazizova G, Loevets T, Vershinina T, Kozyrev I, Gordeev M, Vasichkina E, Pervunina T, Kostareva A.
    BMC Med Genomics; 2020 Nov 20; 13(1):175. PubMed ID: 33218365
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  • 10. Mutation analysis of a large Chinese pedigree with congenital preaxial polydactyly.
    Li H, Wang CY, Wang JX, Wu GS, Yu P, Yan XY, Chen YG, Zhao LH, Zhang YP.
    Eur J Hum Genet; 2009 May 20; 17(5):604-10. PubMed ID: 19066618
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  • 13. Molecular analysis of non-syndromic preaxial polydactyly: preaxial polydactyly type-IV and preaxial polydactyly type-I.
    Fujioka H, Ariga T, Horiuchi K, Otsu M, Igawa H, Kawashima K, Yamamoto Y, Sugihara T, Sakiyama Y.
    Clin Genet; 2005 May 20; 67(5):429-33. PubMed ID: 15811011
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  • 15. Identity-by-descent refines mapping of candidate regions for preaxial polydactyly II /III in a large Chinese pedigree.
    Yang X, Shen Q, Sulaiman X, Liu H, Peng M, Zhang Y.
    Hereditas; 2018 May 20; 155():2. PubMed ID: 28690477
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  • 19. A novel candidate gene for mouse and human preaxial polydactyly with altered expression in limbs of Hemimelic extra-toes mutant mice.
    Clark RM, Marker PC, Kingsley DM.
    Genomics; 2000 Jul 01; 67(1):19-27. PubMed ID: 10945466
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  • 20. The association between preaxial polydactyly and radial longitudinal deficiency in syndromic cases: a report on nine families.
    Al-Qattan MM.
    J Hand Surg Eur Vol; 2018 Sep 01; 43(7):744-750. PubMed ID: 29451098
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