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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

243 related items for PubMed ID: 1308366

  • 1. 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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  • 2. Anomalous inheritance in a kindred with split hand, split foot malformation.
    Spranger M, Schapera J.
    Eur J Pediatr; 1988 Feb 01; 147(2):202-5. PubMed ID: 3366140
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  • 3. Ectrodactyly (split-hand/split-foot) and ectodermal dysplasia with normal lip and palate in a four-generation kindred.
    Wallis CE.
    Clin Genet; 1988 Oct 01; 34(4):252-7. PubMed ID: 3233778
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  • 4. A boy with severe manifestations of type A1 brachydactyly.
    Slavotinek A, Donnai D.
    Clin Dysmorphol; 1998 Jan 01; 7(1):21-7. PubMed ID: 9546826
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  • 5. Anonychia and absence/hypoplasia of distal phalanges (Cooks syndrome): report of a second family.
    Nevin NC, Thomas PS, Eedy DJ, Shepherd C.
    J Med Genet; 1995 Aug 01; 32(8):638-41. PubMed ID: 7473658
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  • 7. Bilateral radial deficiency with lower limb involvement.
    Spranger S, Weber M, Tröger J, Tariverdian G, Opitz JM.
    Am J Med Genet; 1996 May 03; 63(1):193-7. PubMed ID: 8723109
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  • 11. Evidence for autosomal recessive inheritance of split hand/split foot malformation: a report of nine cases.
    Gül D, Oktenli C.
    Clin Dysmorphol; 2002 Jul 03; 11(3):183-6. PubMed ID: 12072797
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  • 12. Autosomal dominant transmission of acrodysostosis.
    Steiner RD, Pagon RA.
    Clin Dysmorphol; 1992 Oct 03; 1(4):201-6. PubMed ID: 1342871
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  • 13. Familial combination of brachydactyly, type E and atrial septal defect, type II.
    Czeizel A, Göblyös P.
    Eur J Pediatr; 1989 Nov 03; 149(2):117-9. PubMed ID: 2591402
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  • 15. Acrodysostosis: autosomal dominant transmission.
    Sheela SR, Perti A, Thomas G.
    Indian Pediatr; 2005 Aug 03; 42(8):822-6. PubMed ID: 16141486
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  • 18. Ectrodactyly with fibular aplasia: a separate entity?
    Menke LA, Bijlsma EK, van Essen AJ, van den Boogaard MJ, van Rijn RR, Cobben JM.
    Eur J Med Genet; 2008 Aug 03; 51(5):488-96. PubMed ID: 18547886
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