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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

105 related items for PubMed ID: 9641152

  • 1. Autosomal dominant hypertension with brachydactyly: an enigmatic form of monogenic hypertension.
    Schuster H.
    Nephrol Dial Transplant; 1998 Jun; 13(6):1337-40. PubMed ID: 9641152
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  • 3. Exclusion of linkage between autosomal dominant split hand/split foot and markers from chromosome 7q: further evidence for genetic heterogeneity.
    Gurrieri F, Genuardi M, Chiurazzi P, Gillessen-Kaesbach G, Neri G.
    Am J Hum Genet; 1994 Oct; 55(4):853-5. PubMed ID: 7942863
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  • 11. Genetics of split hand and split foot. A case study.
    Caldwell BD.
    J Am Podiatr Med Assoc; 1996 Jun; 86(6):244-8. PubMed ID: 8699344
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  • 14. 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; 7(1):29-34. PubMed ID: 9546827
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  • 15. 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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  • 18. New autosomal dominant syndrome reminiscent of Coffin-Siris syndrome and Brachymorphism-Onychodysplasia-Dysphalangism syndrome.
    Elliott AM, Teebi AS.
    Clin Dysmorphol; 2000 Jan 31; 9(1):15-9. PubMed ID: 10649791
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  • 19. A novel homozygous missense mutation in WNT10B in familial split-hand/foot malformation.
    Khan S, Basit S, Zimri FK, Ali N, Ali G, Ansar M, Ahmad W.
    Clin Genet; 2012 Jul 31; 82(1):48-55. PubMed ID: 21554266
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