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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

183 related items for PubMed ID: 12414828

  • 21. Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome.
    Zhao X, Sun M, Zhao J, Leyva JA, Zhu H, Yang W, Zeng X, Ao Y, Liu Q, Liu G, Lo WH, Jabs EW, Amzel LM, Shan X, Zhang X.
    Am J Hum Genet; 2007 Feb; 80(2):361-71. PubMed ID: 17236141
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  • 22. Hemimelic extra toes and Hammer toe are distinct mutations that show a genetic interaction.
    Heus HC, Luijsterburg AJ, van Baren MJ, Breedveld GJ, Joosse MN, Nieuwenhuizen IM, Vermeij-Keers C, Oostra BA, Heutink P.
    Mamm Genome; 2001 Jan; 12(1):77-9. PubMed ID: 11178748
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  • 23. Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated families.
    Akarsu AN, Stoilov I, Yilmaz E, Sayli BS, Sarfarazi M.
    Hum Mol Genet; 1996 Jul; 5(7):945-52. PubMed ID: 8817328
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  • 29. Mutation analysis of HOXD13 gene in a Chinese pedigree with synpolydactyly.
    Dai L, Heng ZC, Zhu J, Cai R, Mao M, Wang H, Lin MJ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun; 22(3):277-80. PubMed ID: 15952114
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  • 33. An acceptor splice site mutation in HOXD13 results in variable hand, but consistent foot malformations.
    Kan SH, Johnson D, Giele H, Wilkie AO.
    Am J Med Genet A; 2003 Aug 15; 121A(1):69-74. PubMed ID: 12900906
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  • 35. [Genotype-phenotype analysis of a Chinese family with split hand/split foot and syndactyly].
    Dai L, Li NN, Deng Y, Mao M, Wang H, Zhu J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug 15; 28(4):379-82. PubMed ID: 21811974
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  • 36. A novel insertion and deletion mutation in the BHLHA9 underlies polydactyly and mesoaxial synostotic syndactyly with phalangeal reduction.
    Ullah A, Ali RH, Majeed AI, Liaqat K, Shah PW, Khan B, Bilal M, Umair M, Ahmad W.
    Eur J Med Genet; 2019 Apr 15; 62(4):278-281. PubMed ID: 30107244
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  • 40. Long-read whole genome sequencing reveals HOXD13 alterations in synpolydactyly.
    Melas M, Kautto EA, Franklin SJ, Mori M, McBride KL, Mosher TM, Pfau RB, Hernandez-Gonzalez ME, McGrath SD, Magrini VJ, White P, Samora JB, Koboldt DC, Wilson RK.
    Hum Mutat; 2022 Feb 15; 43(2):189-199. PubMed ID: 34859533
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