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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

143 related items for PubMed ID: 19591980

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  • 2. 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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  • 3. Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome.
    Goodman FR, Bacchelli C, Brady AF, Brueton LA, Fryns JP, Mortlock DP, Innis JW, Holmes LB, Donnenfeld AE, Feingold M, Beemer FA, Hennekam RC, Scambler PJ.
    Am J Hum Genet; 2000 Jul 15; 67(1):197-202. PubMed ID: 10839976
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  • 5. A missense mutation of HOXA13 underlies hand-foot-genital syndrome in a Chinese family.
    Cao L, Chen C, Leng Y, Yan L, Wang S, Zhang X, Luo Y.
    J Genet; 2017 Sep 15; 96(4):647-652. PubMed ID: 28947713
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  • 6. A novel stable polyalanine [poly(A)] expansion in the HOXA13 gene associated with hand-foot-genital syndrome: proper function of poly(A)-harbouring transcription factors depends on a critical repeat length?
    Utsch B, Becker K, Brock D, Lentze MJ, Bidlingmaier F, Ludwig M.
    Hum Genet; 2002 May 15; 110(5):488-94. PubMed ID: 12073020
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  • 8. Hand-foot-genital syndrome due to a duplication variant in the GC-rich region of HOXA13.
    Geng W, Li F, Zhang R, Cao L, Du X, Gu W, Xu M.
    Eur J Med Genet; 2023 Mar 15; 66(3):104711. PubMed ID: 36702441
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  • 12. 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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  • 15. 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 15; 19(5):573-4. PubMed ID: 11968094
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  • 17. Human HOX gene mutations.
    Goodman FR, Scambler PJ.
    Clin Genet; 2001 Jan 15; 59(1):1-11. PubMed ID: 11206481
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