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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

183 related items for PubMed ID: 12414828

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  • 5. Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences.
    Malik S, Girisha KM, Wajid M, Roy AK, Phadke SR, Haque S, Ahmad W, Koch MC, Grzeschik KH.
    BMC Med Genet; 2007 Dec 11; 8():78. PubMed ID: 18072967
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  • 7. [Genetic analysis of a Chinese pedigree with congenital synpolydactyly].
    Qin W, Shu AL, Xing QH, Yang MS, Feng GY, He L.
    Yi Chuan Xue Bao; 2003 Oct 11; 30(10):973-7. PubMed ID: 14669516
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  • 12. Deletions in HOXD13 segregate with an identical, novel foot malformation in two unrelated families.
    Goodman F, Giovannucci-Uzielli ML, Hall C, Reardon W, Winter R, Scambler P.
    Am J Hum Genet; 1998 Oct 11; 63(4):992-1000. PubMed ID: 9758628
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  • 13. A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactyly.
    Johnson KR, Sweet HO, Donahue LR, Ward-Bailey P, Bronson RT, Davisson MT.
    Hum Mol Genet; 1998 Jun 11; 7(6):1033-8. PubMed ID: 9580668
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  • 15. [Synpolydactyly in a Chinese kindred: mutation detection, prenatal ultrasonographic and molecular diagnosis].
    Jin H, Lin PF, Wang QM, Mao F, Cai Y, Gong YQ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec 11; 28(6):601-5. PubMed ID: 22161087
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  • 16. Limb malformations and the human HOX genes.
    Goodman FR.
    Am J Med Genet; 2002 Oct 15; 112(3):256-65. PubMed ID: 12357469
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  • 17. Molecular characterization of HOXA13 polyalanine expansion proteins in hand-foot-genital syndrome.
    Utsch B, McCabe CD, Galbraith K, Gonzalez R, Born M, Dötsch J, Ludwig M, Reutter H, Innis JW.
    Am J Med Genet A; 2007 Dec 15; 143A(24):3161-8. PubMed ID: 17935235
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  • 19. Identification of a missense HOXD13 mutation in a Chinese family with syndactyly type I-c using exome sequencing.
    Deng H, Tan T, He Q, Lin Q, Yang Z, Zhu A, Guan L, Xiao J, Song Z, Guo Y.
    Mol Med Rep; 2017 Jul 15; 16(1):473-477. PubMed ID: 28498426
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