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Journal Abstract Search

318 related items for PubMed ID: 8209882

  • 1. Parental consanguinity in two sibs with omodysplasia.
    Baxová A, Maroteaux P, Barosová J, Netriová I.
    Am J Med Genet; 1994 Feb 01; 49(3):263-5. PubMed ID: 8209882
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  • 2. Familial congenital micromelic dysplasia with dislocation of radius and distinct face: a new skeletal dysplasia syndrome.
    Borochowitz Z, Barak M, Hershkowitz S.
    Am J Med Genet; 1991 Apr 01; 39(1):91-6. PubMed ID: 1867270
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  • 4. Dyggve-Melchior-Clausen syndrome: genetic studies and report of affected sibs.
    Toledo SP, Saldanha PH, Lamego C, Mourão PA, Dietrich CP, Mattar E.
    Am J Med Genet; 1979 Apr 01; 4(3):255-61. PubMed ID: 117710
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  • 6. Autosomal recessive omodysplasia.
    al Gazali LI, Abou al-Asaad F.
    Clin Dysmorphol; 1995 Jan 01; 4(1):52-6. PubMed ID: 7735505
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  • 7. Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variant.
    Franceschini P, Testa A, Bogetti G, Girardo E, Guala A, Lopez-Bell G, Buzio G, Ferrario E, Piccato E.
    Am J Med Genet; 1992 Jan 01; 42(1):112-6. PubMed ID: 1308349
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  • 8. Familial rhizomelic dysplasia: phenotypic variation or heterogeneity?
    Viljoen D, Goldblatt J, Wallis C, Beighton P.
    Am J Med Genet; 1987 Apr 01; 26(4):941-7. PubMed ID: 3591839
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  • 10. Short rib-polydactyly syndrome, Majewski type.
    Chen H, Yang SS, Gonzalez E, Fowler M, Al Saadi A.
    Am J Med Genet; 1980 Apr 01; 7(2):215-22. PubMed ID: 7468649
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  • 13. Deafness, onycho-osteodystrophy, mental retardation (DOOR) syndrome.
    Nevin NC, Thomas PS, Calvert J, Reid MM.
    Am J Med Genet; 1982 Nov 01; 13(3):325-32. PubMed ID: 7180877
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  • 14. An autosomal recessive form of lethal chondrodystrophy with severe thoracic narrowing, rhizoacromelic type of micromelia, polydacytly and genital anomalies.
    Verma IC, Bhargava S, Agarwal S.
    Birth Defects Orig Artic Ser; 1975 Nov 01; 11(6):167-74. PubMed ID: 1103993
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  • 16. Metaphyseal dysostosis, conductive hearing loss and mental retardation: a recessively inherited syndrome.
    Rimoin DL, McAlister WH.
    Birth Defects Orig Artic Ser; 1971 Mar 01; 07(4):116-22. PubMed ID: 5173335
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  • 17. Hirsutism-skeletal dysplasia-mental retardation syndrome with abnormal face and a uric acid metabolism disorder.
    Wiedemann HR, Oldigs HD, Oppermann HC, Oster O.
    Am J Med Genet; 1993 Jun 01; 46(4):403-9. PubMed ID: 8357012
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