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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

273 related items for PubMed ID: 9546826

  • 1. A boy with severe manifestations of type A1 brachydactyly.
    Slavotinek A, Donnai D.
    Clin Dysmorphol; 1998 Jan; 7(1):21-7. PubMed ID: 9546826
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  • 2. Cooks syndrome: a case report and brief review.
    Brennan CB, Buehler T, Lesher JL.
    Pediatr Dermatol; 2013 Jan; 30(4):e52-3. PubMed ID: 22329539
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  • 5. Hands and feet in the Apert syndrome.
    Cohen MM, Kreiborg S.
    Am J Med Genet; 1995 May 22; 57(1):82-96. PubMed ID: 7645606
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  • 7. Autosomal dominant inheritance of tetramelic monodactyly.
    Sommer A, Hines SJ.
    Am J Med Genet; 1992 Jan 01; 42(1):51-4. PubMed ID: 1308366
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  • 8. Clinical and locus heterogeneity in brachydactyly type C.
    Robin NH, Gunay-Aygun M, Polinkovsky A, Warman ML, Morrison S.
    Am J Med Genet; 1997 Jan 31; 68(3):369-77. PubMed ID: 9024575
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  • 11. Tibial hemimelia: report on 37 new cases, clinical and genetic considerations.
    Richieri-Costa A, Ferrareto I, Masiero D, da Silva CR.
    Am J Med Genet; 1987 Aug 31; 27(4):867-84. PubMed ID: 3425598
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  • 13. Familial distal arthrogryposis type I.
    Stoll C, Alembik Y, Dott B.
    Ann Genet; 1996 Aug 31; 39(2):75-80. PubMed ID: 8766137
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  • 17. An unusual family with brachydactyly.
    Silva EO.
    Am J Med Genet A; 2003 Mar 01; 117A(2):191-3. PubMed ID: 12567422
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  • 20. Split hand/split foot anomaly in a family segregating a balanced translocation with breakpoint on 7q22.1.
    Genuardi M, Pomponi MG, Sammito V, Bellussi A, Zollino M, Neri G.
    Am J Med Genet; 1993 Nov 01; 47(6):823-31. PubMed ID: 8279479
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