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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

160 related items for PubMed ID: 6705252

  • 21. A postaxial polydactyly and progressive myopia syndrome of autosomal dominant origin.
    Czeizel A, Brooser G.
    Clin Genet; 1986 Nov; 30(5):406-8. PubMed ID: 3802559
    [Abstract] [Full Text] [Related]

  • 22. ZRS 406A>G mutation in patients with tibial hypoplasia, polydactyly and triphalangeal first fingers.
    Norbnop P, Srichomthong C, Suphapeetiporn K, Shotelersuk V.
    J Hum Genet; 2014 Aug; 59(8):467-70. PubMed ID: 24965254
    [Abstract] [Full Text] [Related]

  • 23. Confirmation of genetic homogeneity of syndactyly type IV and triphalangeal thumb-polysyndactyly syndrome in a Chinese family and review of the literature.
    Dai L, Guo H, Meng H, Zhang K, Hu H, Yao H, Bai Y.
    Eur J Pediatr; 2013 Nov; 172(11):1467-73. PubMed ID: 23793141
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  • 25. 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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  • 26. Polydactyly: report of a large kindred.
    Kirkland LR, Russell RO.
    South Med J; 1976 Apr 03; 69(4):436-7. PubMed ID: 1265503
    [Abstract] [Full Text] [Related]

  • 27. Aplasia of tibia with split-hand/split-foot deformity. Report of six families with 35 cases and considerations about variability and penetrance.
    Majewski F, Küster W, ter Haar B, Goecke T.
    Hum Genet; 1985 Apr 03; 70(2):136-47. PubMed ID: 4007857
    [Abstract] [Full Text] [Related]

  • 28. Phocomelia, flexion deformities and absent thumbs: a new hereditary upper limb malformation.
    Holmes LB, Borden S.
    Pediatrics; 1974 Oct 03; 54(4):461-5. PubMed ID: 4415048
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  • 31. Two novel point mutations in the long-range SHH enhancer in three families with triphalangeal thumb and preaxial polydactyly.
    Gurnett CA, Bowcock AM, Dietz FR, Morcuende JA, Murray JC, Dobbs MB.
    Am J Med Genet A; 2007 Jan 01; 143A(1):27-32. PubMed ID: 17152067
    [Abstract] [Full Text] [Related]

  • 32. An autosomal dominant syndrome of radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema.
    Schmitt E, Gillenwater JY, Kelly TE.
    Am J Med Genet; 1982 Sep 01; 13(1):63-9. PubMed ID: 7137222
    [Abstract] [Full Text] [Related]

  • 33. An Indian family with postaxial polydactyly in four generations.
    Kucheria K, Kenue RK, Taneja N.
    Clin Genet; 1981 Jul 01; 20(1):36-9. PubMed ID: 7296946
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  • 35. [Syndactylia, polydactylia and absence of thumbs associated with tibial hypoplasia and a nose abnormality in 2 generations: a new syndrome].
    Canki N.
    Rev Med Liege; 1980 Jun 01; 35(11):464-7. PubMed ID: 6256840
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  • 38. Autosomal dominant tibial hemimelia-polysyndactyly-triphalangeal thumbs syndrome: report of a Brazilian family.
    Richieri-Costa A, de Miranda E, Kamiya TY, Freire-Maia DV.
    Am J Med Genet; 1990 May 01; 36(1):1-6. PubMed ID: 2333896
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  • 40. [Multiple synostosis].
    Czeizel E, Göblyös P.
    Orv Hetil; 1993 Aug 29; 134(35):1917-20. PubMed ID: 8395675
    [Abstract] [Full Text] [Related]

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