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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

199 related items for PubMed ID: 2551554

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  • 3. Brachydactyly with absence of middle phalanges and hypoplastic nails. A new hereditary syndrome.
    Cuevas-Sosa A, García-Segur F.
    J Bone Joint Surg Br; 1971 Feb; 53(1):101-5. PubMed ID: 4325377
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  • 5. The Greig cephalopolysyndactyly syndrome in a Canadian family.
    Chudley AE, Houston CS.
    Am J Med Genet; 1982 Nov; 13(3):269-76. PubMed ID: 6295159
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  • 7. Poly-syndactyly of hands and feet with talipes equino-varus. An unusual combination.
    Gadegone WM, Kumar K.
    J Hand Surg Br; 1984 Jun; 9(2):149-50. PubMed ID: 6086792
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  • 8. [Synpolydactyly: unusual features and variable expression in 5 generations of an Italian family].
    Chessa Ricotti G, Lapi E, De Bernardi A, Corti P.
    Pediatr Med Chir; 1990 Jun; 12(3):259-63. PubMed ID: 2177188
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  • 9. A hereditable combination of congenital anomalies.
    Agarwal RP, Jain D, Ramesh Babu CS, Garg RK.
    J Bone Joint Surg Br; 1996 May; 78(3):492-4. PubMed ID: 8636194
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  • 10. Oculodentodigital dysplasia.
    Fára M, Horák I, Hrivnáková J, Kapras J, Nová M, Stloukalová M.
    Acta Chir Plast; 1977 May; 19(2):110-22. PubMed ID: 74156
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  • 13. Proximal symphalangism, hyperopia, conductive hearing impairment, and the NOG gene: 2 new mutations.
    Thomeer HG, Admiraal RJ, Hoefsloot L, Kunst HP, Cremers CW.
    Otol Neurotol; 2011 Jun; 32(4):632-8. PubMed ID: 21358557
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  • 16. Autosomal dominant syndrome of camptodactyly, clinodactyly, syndactyly, and bifid toes.
    Malik S, Afzal M, Gul S, Wahab A, Ahmad M.
    Am J Med Genet A; 2010 Sep; 152A(9):2313-7. PubMed ID: 20683984
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