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PUBMED FOR HANDHELDS

Journal Abstract Search

270 related items for PubMed ID: 16005596

  • 1. Variable hand and foot abnormalities in family with congenital vertical talus and CDMP-1 gene mutation.
    Dobbs MB, Gurnett CA, Robarge J, Gordon JE, Morcuende JA, Bowcock AM.
    J Orthop Res; 2005 Nov; 23(6):1490-4. PubMed ID: 16005596
    [Abstract] [Full Text] [Related]

  • 2. The mutational spectrum of brachydactyly type C.
    Everman DB, Bartels CF, Yang Y, Yanamandra N, Goodman FR, Mendoza-Londono JR, Savarirayan R, White SM, Graham JM, Gale RP, Svarch E, Newman WG, Kleckers AR, Francomano CA, Govindaiah V, Singh L, Morrison S, Thomas JT, Warman ML.
    Am J Med Genet; 2002 Oct 15; 112(3):291-6. PubMed ID: 12357473
    [Abstract] [Full Text] [Related]

  • 3. Broad phenotypic spectrum caused by an identical heterozygous CDMP-1 mutation in three unrelated families.
    Savarirayan R, White SM, Goodman FR, Graham JM, Delatycki MB, Lachman RS, Rimoin DL, Everman DB, Warman ML.
    Am J Med Genet A; 2003 Mar 01; 117A(2):136-42. PubMed ID: 12567410
    [Abstract] [Full Text] [Related]

  • 4. Frameshift mutation in the cartilage-derived morphogenetic protein 1 (CDMP1) gene and severe acromesomelic chondrodysplasia resembling Grebe-type chondrodysplasia.
    Faiyaz-Ul-Haque M, Ahmad W, Wahab A, Haque S, Azim AC, Zaidi SH, Teebi AS, Ahmad M, Cohn DH, Siddique T, Tsui LC.
    Am J Med Genet; 2002 Jul 22; 111(1):31-7. PubMed ID: 12124730
    [Abstract] [Full Text] [Related]

  • 5. Autosomal dominant transmission of isolated congenital vertical talus.
    Stern HJ, Clark RD, Stroberg AJ, Shohat M.
    Clin Genet; 1989 Dec 22; 36(6):427-30. PubMed ID: 2591068
    [Abstract] [Full Text] [Related]

  • 6. HOXD10 M319K mutation in a family with isolated congenital vertical talus.
    Dobbs MB, Gurnett CA, Pierce B, Exner GU, Robarge J, Morcuende JA, Cole WG, Templeton PA, Foster B, Bowcock AM.
    J Orthop Res; 2006 Mar 22; 24(3):448-53. PubMed ID: 16450407
    [Abstract] [Full Text] [Related]

  • 7. Association of external auditory canal atresia, vertical talus, and hypertelorism: confirmation of Rasmussen syndrome.
    Julia S, Pedespan JM, Boudard P, Barbier R, Gavilan-Cellie I, Chateil JF, Lacombe D.
    Am J Med Genet; 2002 Jun 15; 110(2):179-81. PubMed ID: 12116258
    [Abstract] [Full Text] [Related]

  • 8. A HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth disease.
    Shrimpton AE, Levinsohn EM, Yozawitz JM, Packard DS, Cady RB, Middleton FA, Persico AM, Hootnick DR.
    Am J Hum Genet; 2004 Jul 15; 75(1):92-6. PubMed ID: 15146389
    [Abstract] [Full Text] [Related]

  • 9. Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1.
    Thomas JT, Kilpatrick MW, Lin K, Erlacher L, Lembessis P, Costa T, Tsipouras P, Luyten FP.
    Nat Genet; 1997 Sep 15; 17(1):58-64. PubMed ID: 9288098
    [Abstract] [Full Text] [Related]

  • 10. Congenital vertical talus and its familial occurrence: an analysis of 36 patients.
    Ogata K, Schoenecker PL, Sheridan J.
    Clin Orthop Relat Res; 1979 Sep 15; (139):128-32. PubMed ID: 455829
    [Abstract] [Full Text] [Related]

  • 11. A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2.
    Kjaer KW, Eiberg H, Hansen L, van der Hagen CB, Rosendahl K, Tommerup N, Mundlos S.
    J Med Genet; 2006 Mar 15; 43(3):225-31. PubMed ID: 16014698
    [Abstract] [Full Text] [Related]

  • 12. Magnetic resonance angiography in clubfoot and vertical talus: a feasibility study.
    Kruse L, Gurnett CA, Hootnick D, Dobbs MB.
    Clin Orthop Relat Res; 2009 May 15; 467(5):1250-5. PubMed ID: 19127394
    [Abstract] [Full Text] [Related]

  • 13. Congenital vertical talus.
    Benard MA.
    Clin Podiatr Med Surg; 2000 Jul 15; 17(3):471-80, vii. PubMed ID: 10943500
    [Abstract] [Full Text] [Related]

  • 14. Congenital vertical talus: a review.
    McKie J, Radomisli T.
    Clin Podiatr Med Surg; 2010 Jan 15; 27(1):145-56. PubMed ID: 19963176
    [Abstract] [Full Text] [Related]

  • 15. Mutations in GDF5 presenting as semidominant brachydactyly A1.
    Byrnes AM, Racacho L, Nikkel SM, Xiao F, MacDonald H, Underhill TM, Bulman DE.
    Hum Mutat; 2010 Oct 15; 31(10):1155-62. PubMed ID: 20683927
    [Abstract] [Full Text] [Related]

  • 16. [A DNA duplication at chromosome 10q24.3 is associated with split-hand split-foot malformation in a Chinese family].
    Yang W, Hu ZJ, Yu XF, Li QH, Zhang AJ, Deng X, Zhang AY, Gao CS, Liu Y, Ao Y, Lo WH, Zhang X.
    Zhonghua Yi Xue Za Zhi; 2006 Mar 14; 86(10):652-8. PubMed ID: 16681918
    [Abstract] [Full Text] [Related]

  • 17. Brachydactyly type A1 with abnormal menisci and scoliosis in three generations.
    Raff ML, Leppig KA, Rutledge JC, Weinberger E, Pagon RA.
    Clin Dysmorphol; 1998 Jan 14; 7(1):29-34. PubMed ID: 9546827
    [Abstract] [Full Text] [Related]

  • 18. On the inheritance of the split hand/split foot malformation.
    Zlotogora J.
    Am J Med Genet; 1994 Oct 15; 53(1):29-32. PubMed ID: 7802032
    [Abstract] [Full Text] [Related]

  • 19. Congenital vertical talus in four generations of the same family.
    Levinsohn EM, Shrimpton AE, Cady RB, Packard DS, Hootnick DR.
    Skeletal Radiol; 2004 Nov 15; 33(11):649-54. PubMed ID: 15368082
    [Abstract] [Full Text] [Related]

  • 20. Mutation of HOXA13 in hand-foot-genital syndrome.
    Mortlock DP, Innis JW.
    Nat Genet; 1997 Feb 15; 15(2):179-80. PubMed ID: 9020844
    [Abstract] [Full Text] [Related]

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