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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

144 related items for PubMed ID: 9072822

  • 1. HOX gene links limb, genital defects.
    Dickman S.
    Science; 1997 Mar 14; 275(5306):1568. PubMed ID: 9072822
    [No Abstract] [Full Text] [Related]

  • 2. Human HOX gene mutations.
    Goodman FR, Scambler PJ.
    Clin Genet; 2001 Jan 14; 59(1):1-11. PubMed ID: 11206481
    [Abstract] [Full Text] [Related]

  • 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 14; 67(1):197-202. PubMed ID: 10839976
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  • 5. Mutation of HOXA13 in hand-foot-genital syndrome.
    Mortlock DP, Innis JW.
    Nat Genet; 1997 Feb 14; 15(2):179-80. PubMed ID: 9020844
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  • 6. Triphalangeal thumbs with brachyectrodactyly: a sporadic case.
    Brown AM, Romness M, Dong DA, Kelly TE.
    Am J Med Genet A; 2008 Nov 01; 146A(21):2835-6. PubMed ID: 18924168
    [No Abstract] [Full Text] [Related]

  • 7. [Hand-foot-genital syndrome].
    Mitsubuchi H, Endo F.
    Nihon Rinsho; 2006 Jun 28; Suppl 2():647-8. PubMed ID: 16817484
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  • 9. 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 28; 17(2):e28-30. PubMed ID: 21549968
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  • 10. 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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  • 15. Hand-foot-genital syndrome: the importance of hallux varus.
    Cleveland RH, Holmes LB.
    Pediatr Radiol; 1990 Oct 15; 20(5):339-43. PubMed ID: 2349017
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  • 17. Hand-foot-genital syndrome with a 7p15 deletion: clinically recognizable syndrome.
    Hosoki K, Ohta T, Fujita K, Nishigaki S, Shiomi M, Niikawa N, Saitoh S.
    Pediatr Int; 2012 Jun 15; 54(3):e22-5. PubMed ID: 22631585
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  • 18. Al-Awadi-Raas-Rothschild (limb/pelvis/uterus-hypoplasia/aplasia) syndrome and WNT7A mutations: genetic homogeneity and nosological delineation.
    Garavelli L, Wischmeijer A, Rosato S, Gelmini C, Reverberi S, Sassi S, Ferrari A, Mari F, Zabel B, Lausch E, Unger S, Superti-Furga A.
    Am J Med Genet A; 2011 Feb 15; 155A(2):332-6. PubMed ID: 21271649
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  • 19. The hand-foot-genital syndrome: on the variable expression in affected males.
    Fryns JP, Vogels A, Decock P, van den Berghe H.
    Clin Genet; 1993 May 15; 43(5):232-4. PubMed ID: 8375102
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  • 20. 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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