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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

221 related items for PubMed ID: 11206481

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  • 2. 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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  • 4. Severe manifestations of hand-foot-genital syndrome associated with a novel HOXA13 mutation.
    Imagawa E, Kayserili H, Nishimura G, Nakashima M, Tsurusaki Y, Saitsu H, Ikegawa S, Matsumoto N, Miyake N.
    Am J Med Genet A; 2014 Sep 15; 164A(9):2398-402. PubMed ID: 24934387
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  • 5. Novel mutations of the HOXD13 gene in hand and foot malformations.
    Nakano K, Sakai N, Yamazaki Y, Watanabe H, Yamada N, Sezaki K, Susami T, Tokunaga K, Takato T, Uchinuma E.
    Int Surg; 2007 Sep 15; 92(5):287-95. PubMed ID: 18399101
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  • 6. 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 15; 7(6):1033-8. PubMed ID: 9580668
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  • 7. Hallux valgus interphalangeus and a novel mutation in HOXA13. Part of the broadening spectrum of Hand-Foot-Genital syndrome.
    Parker L, Mangwani J, Wakeling E, Singh D.
    Foot Ankle Surg; 2011 Jun 15; 17(2):e28-30. PubMed ID: 21549968
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  • 12. HOX gene links limb, genital defects.
    Dickman S.
    Science; 1997 Mar 14; 275(5306):1568. PubMed ID: 9072822
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  • 13. Familial deletion of the HOXA gene cluster associated with Hand-Foot-Genital syndrome and phenotypic variability.
    Tas E, Sebastian J, Madan-Khetarpal S, Sweet P, Yatsenko AN, Pollock N, Rajkovic A, Schneck FX, Yatsenko SA, Witchel SF.
    Am J Med Genet A; 2017 Jan 14; 173(1):221-224. PubMed ID: 27649277
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  • 14. 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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  • 15. Mutation of HOXA13 in hand-foot-genital syndrome.
    Mortlock DP, Innis JW.
    Nat Genet; 1997 Feb 15; 15(2):179-80. PubMed ID: 9020844
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  • 17. [Hand-foot-genital syndrome].
    Mitsubuchi H, Endo F.
    Nihon Rinsho; 2006 Jun 28; Suppl 2():647-8. PubMed ID: 16817484
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  • 19. A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome.
    Innis JW, Goodman FR, Bacchelli C, Williams TM, Mortlock DP, Sateesh P, Scambler PJ, McKinnon W, Guttmacher AE.
    Hum Mutat; 2002 May 28; 19(5):573-4. PubMed ID: 11968094
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