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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

273 related items for PubMed ID: 9546826

  • 21. Greig cephalopolysyndactyly syndrome in a large family: a comparison of the clinical signs with those described in the literature.
    Ausems MG, Ippel PF, Renardel de Lavalette PA.
    Clin Dysmorphol; 1994 Jan; 3(1):21-30. PubMed ID: 8205322
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  • 22. Brachydactyly type B1: report of a family with de novo ROR2 mutation.
    Hamamy H, Saleh N, Oldridge M, Al-Hadidy A, Ajlouni K.
    Clin Genet; 2006 Dec; 70(6):538-40. PubMed ID: 17101003
    [No Abstract] [Full Text] [Related]

  • 23. Anomalous inheritance in a kindred with split hand, split foot malformation.
    Spranger M, Schapera J.
    Eur J Pediatr; 1988 Feb; 147(2):202-5. PubMed ID: 3366140
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  • 24. Retinitis pigmentosa, mental retardation, marked short stature, and brachydactyly in two sibs.
    Lorda-Sanchez I, Trujillo MJ, Gimenez A, Garcia-Sandoval B, Franco A, Sanz R, Rodriguez de Alba M, Ramos C, Ayuso C.
    Ophthalmic Genet; 1999 Jun; 20(2):127-31. PubMed ID: 10420199
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  • 25. A novel type of autosomal recessive syndactyly: clinical and molecular studies in a family of Pakistani origin.
    Malik S, Arshad M, Amin-Ud-Din M, Oeffner F, Dempfle A, Haque S, Koch MC, Ahmad W, Grzeschik KH.
    Am J Med Genet A; 2004 Apr 01; 126A(1):61-7. PubMed ID: 15039974
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  • 26. Familial digital arthropathy-brachydactyly.
    Amor DJ, Tudball C, Gardner RJ, Lamandé SR, Bateman JF, Savarirayan R.
    Am J Med Genet; 2002 Mar 15; 108(3):235-40. PubMed ID: 11891693
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  • 27. Catel-Manzke syndrome without cleft palate: a case report.
    Puri RD, Phadke SR.
    Clin Dysmorphol; 2003 Oct 15; 12(4):279-81. PubMed ID: 14564220
    [Abstract] [Full Text] [Related]

  • 28. Acrodysostosis in two generations: an autosomal dominant syndrome.
    Hernández RM, Miranda A, Kofman-Alfaro S.
    Clin Genet; 1991 May 15; 39(5):376-82. PubMed ID: 1860254
    [Abstract] [Full Text] [Related]

  • 29. Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second family.
    Meinecke P.
    Genet Couns; 1993 May 15; 4(2):147-51. PubMed ID: 8395190
    [Abstract] [Full Text] [Related]

  • 30. Further evidence for germinal mosaicism in cleft hand/cleft foot syndrome. Two affected halfsisters and normal father.
    De Smet L, Devriendt K, Fryns JP.
    Genet Couns; 2001 May 15; 12(3):251-4. PubMed ID: 11693788
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  • 32. Brachydactyly-short stature-hypertension (Bilginturan) syndrome: report on two families.
    Chitayat D, Grix A, Balfe JW, Abramowicz JS, Garza J, Fong CT, Silver MM, Saller DN, Bresnick GH, Giedion A, Lachman RS, Rimoin DL.
    Am J Med Genet; 1997 Dec 19; 73(3):279-85. PubMed ID: 9415685
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  • 34. Ectrodactyly (split-hand/split-foot) and ectodermal dysplasia with normal lip and palate in a four-generation kindred.
    Wallis CE.
    Clin Genet; 1988 Oct 19; 34(4):252-7. PubMed ID: 3233778
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  • 37. Syndactyly type IV/hexadactyly of feet associated with unilateral absence of the tibia.
    Rambaud-Cousson A, Dudin AA, Zuaiter AS, Thalji A.
    Am J Med Genet; 1991 Aug 01; 40(2):144-5. PubMed ID: 1654744
    [Abstract] [Full Text] [Related]

  • 38. Is brachydactyly type Ballard a variant of brachydactyly type E?
    Jensen K, Hoo JJ.
    Am J Med Genet A; 2004 Aug 15; 129A(1):95-7. PubMed ID: 15266625
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