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Journal Abstract Search


258 related items for PubMed ID: 3568429

  • 21. Absent tibiae--polydactyly--triphalangeal thumbs with fibular dimelia: variable expression of the Werner (McKusick 188770) syndrome?
    Vargas FR, Pontes RL, Llerena Júnior JC, de Almeida JC.
    Am J Med Genet; 1995 Jan 30; 55(3):261-4. PubMed ID: 7726219
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  • 22. Dominant inheritance of a syndrome similar to Rubinstein-Taybi.
    Cotsirilos P, Taylor JC, Matalon R.
    Am J Med Genet; 1987 Jan 30; 26(1):85-93. PubMed ID: 3812583
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  • 24. Autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias.
    Guttmacher AE.
    Am J Med Genet; 1993 Apr 15; 46(2):219-22. PubMed ID: 8484413
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  • 25. Polydactyly: a study of a five generation Indian family.
    Radhakrishna U, Multani AS, Solanki JV, Shah VC, Chinoy NJ.
    J Med Genet; 1993 Apr 15; 30(4):296-9. PubMed ID: 8487274
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  • 26. Two rare cases of association of thumb hypoplasia and polydactyly of the homolateral foot.
    Philandrianos C, Salazard B, Casanova D.
    J Hand Surg Eur Vol; 2009 Feb 15; 34(1):125-7. PubMed ID: 19129363
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  • 27. A case of symbrachydactyly with oligodactyly.
    Seven M, Yuksel A, Ozkilic A.
    Genet Couns; 2001 Feb 15; 12(1):77-83. PubMed ID: 11332981
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  • 30. Acro-renal-ocular syndrome: autosomal dominant thumb hypoplasia, renal ectopia, and eye defect.
    Halal F, Homsy M, Perreault G.
    Am J Med Genet; 1984 Apr 15; 17(4):753-62. PubMed ID: 6426304
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  • 32. Mutational analysis of HOXD13 and HOXA13 genes in the triphalangeal thumb-brachyectrodactyly syndrome.
    Pérez-Cabrera A, Kofman-Alfaro S, Zenteno JC.
    J Orthop Res; 2002 Sep 15; 20(5):899-901. PubMed ID: 12382951
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  • 33. Phenotypic variability of triphalangeal thumb-polysyndactyly syndrome linked to chromosome 7q36.
    Balci S, Demirtas M, Civelek B, Piskin M, Sensoz O, Akarsu AN.
    Am J Med Genet; 1999 Dec 22; 87(5):399-406. PubMed ID: 10594878
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  • 34. Triphalangeal thumb.
    Miura T.
    Plast Reconstr Surg; 1976 Nov 22; 58(5):587-94. PubMed ID: 981404
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  • 35. Dilemmas in counselling: the EEC syndrome.
    Tse K, Temple IK, Baraitser M.
    J Med Genet; 1990 Dec 22; 27(12):752-5. PubMed ID: 2074560
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  • 37. Localization of dominantly inherited isolated triphalangeal thumb to chromosomal region 7q36.
    Dobbs MB, Dietz FR, Gurnett CA, Morcuende JA, Steyers CM, Murray JC.
    J Orthop Res; 2000 May 22; 18(3):340-4. PubMed ID: 10937618
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  • 38. A hereditable combination of congenital anomalies.
    Agarwal RP, Jain D, Ramesh Babu CS, Garg RK.
    J Bone Joint Surg Br; 1996 May 22; 78(3):492-4. PubMed ID: 8636194
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