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Journal Abstract Search

156 related items for PubMed ID: 8588578

  • 1. Achondrogenesis type II with polydactyly.
    Rittler M, Orioli IM.
    Am J Med Genet; 1995 Nov 06; 59(2):157-60. PubMed ID: 8588578
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  • 4. Achondrogenesis type II (Langer-Saldino)--a case report.
    Swar MO, Srikrishna BV.
    Afr J Med Med Sci; 1995 Sep 06; 24(3):297-9. PubMed ID: 8798967
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  • 13. Hydrometrocolpos and polydactyly: a common neonatal presentation of Bardet-Biedl and McKusick-Kaufman syndromes.
    David A, Bitoun P, Lacombe D, Lambert JC, Nivelon A, Vigneron J, Verloes A.
    J Med Genet; 1999 Aug 06; 36(8):599-603. PubMed ID: 10465109
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  • 15. Persistence of müllerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly, renal and craniofacial anomalies.
    Urioste M, Rodríguez JI, Barcia JM, Martín M, Escribá R, Pardo M, Camino J, Martínez-Frías ML.
    Am J Med Genet; 1993 Sep 15; 47(4):494-503. PubMed ID: 8256813
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  • 16. Jeune syndrome with tongue lobulation and preaxial polydactyly, and Jeune syndrome with situs inversus and asplenia: compound heterozygosity Jeune-Mohr and Jeune-Ivemark?
    Majewski E, Oztürk B, Gillessen-Kaesbach G.
    Am J Med Genet; 1996 May 03; 63(1):74-9. PubMed ID: 8723090
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  • 18. The Mckusick-Kaufman syndrome: report of a case with some associations.
    Kotiloğlu E, Kaya H, Güney I, Balci S.
    Turk J Pediatr; 2002 May 03; 44(2):176-9. PubMed ID: 12026212
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