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Journal Abstract Search

218 related items for PubMed ID: 8831130

  • 1. Chorioretinal dysplasia-microcephaly-mental retardation syndrome: another family with autosomal dominant inheritance.
    Hordijk R, Van de Logt F, Houtman WA, Van Essen AJ.
    Genet Couns; 1996; 7(2):113-22. PubMed ID: 8831130
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  • 3. [Ophthalmological findings in microcephaly-lymphoedema-chorioretinal dysplasia syndrome].
    Hatt Brupbacher SC, Job O, Senn P, Dedes W.
    Klin Monbl Augenheilkd; 2009 Apr; 226(4):344-6. PubMed ID: 19384796
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  • 5. Microcephaly-lymphedema-chorioretinal dysplasia: a unique genetic syndrome with variable expression and possible characteristic facial appearance.
    Limwongse C, Wyszynski RE, Dickerman LH, Robin NH.
    Am J Med Genet; 1999 Sep 17; 86(3):215-8. PubMed ID: 10482868
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  • 7. Autosomal dominant microcephaly with mental retardation.
    Bawle E, Horton M.
    Am J Med Genet; 1989 Jul 17; 33(3):382-4. PubMed ID: 2801773
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  • 10. Syndrome of microcephaly, Brachmann-de Lange-like facial changes, severe metatarsus adductus, and developmental delay: mild Brachmann-de Lange syndrome?
    Halal F, Silver K.
    Am J Med Genet; 1992 Feb 01; 42(3):381-6. PubMed ID: 1536185
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  • 12. A syndrome of microcephaly, mental retardation, unusual facies, cleft palate, and weight deficiency.
    Weaver DD, Williams CP.
    Birth Defects Orig Artic Ser; 1977 Feb 01; 13(3B):69-84. PubMed ID: 890101
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  • 13. Microcephaly, lymphedema, and chorioretinal dysplasia: report of two additional cases.
    Angle B, Holgado S, Burton BK, Miller MT, Shapiro MJ, Opitz JM.
    Am J Med Genet; 1994 Nov 01; 53(2):99-101. PubMed ID: 7856652
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  • 14. Autosomal dominant inheritance in Setleis syndrome.
    Masuno M, Imaizumi K, Makita Y, Nakamura M, Kuroki Y.
    Am J Med Genet; 1995 May 22; 57(1):57-60. PubMed ID: 7645599
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  • 15. Vertical transmission of the Ohdo blepharophimosis syndrome.
    Mhanni AA, Dawson AJ, Chudley AE.
    Am J Med Genet; 1998 May 01; 77(2):144-8. PubMed ID: 9605288
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  • 16. Lissencephaly and mild cerebellar vermis hypoplasia in a case of microcephaly and chorioretinal dysplasia.
    Lee BJ, Kim JH, Yu YS.
    Ophthalmic Genet; 2010 Jun 01; 31(2):89-93. PubMed ID: 20450312
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  • 19. Zimmermann-Laband syndrome in a patient with severe mental retardation.
    Van Buggenhout GJ, Brunner HG, Trommelen JC, Hamel BC.
    Genet Couns; 1995 Jun 01; 6(4):321-7. PubMed ID: 8775419
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  • 20. [Microcephalia vera. Genetic heterogeneity and mental retardation].
    Baldellou Váquez A, Caro Rebollo J, Bernad Usoz JV, Tamparillas Salvador M.
    An Esp Pediatr; 1988 Nov 01; 29(5):397-400. PubMed ID: 3232899
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