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Journal Abstract Search

154 related items for PubMed ID: 7977454

  • 1. Chorioretinal dysplasia-microcephaly-mental retardation syndrome.
    Warburg M, Heuer HE.
    Am J Med Genet; 1994 Aug 01; 52(1):117. PubMed ID: 7977454
    [No Abstract] [Full Text] [Related]

  • 2. [Ophthalmological findings in microcephaly-lymphoedema-chorioretinal dysplasia syndrome].
    Hatt Brupbacher SC, Job O, Senn P, Dedes W.
    Klin Monbl Augenheilkd; 2009 Apr 01; 226(4):344-6. PubMed ID: 19384796
    [Abstract] [Full Text] [Related]

  • 3. 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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  • 5. Chorioretinal dysplasia-microcephaly-mental retardation syndrome: report of an American family.
    Sadler LS, Robinson LK.
    Am J Med Genet; 1993 Aug 01; 47(1):65-8. PubMed ID: 8368255
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  • 6. 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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  • 8. [Hereditary microcephaly with autosomal dominant chorioretinal dysplasia (author's transl)].
    Alzial C, Dufier JL, Brasnu C, Aicardi J, de Grouchy J.
    Sem Hop; 1999 Sep 17; 57(1-2):43-6. PubMed ID: 6258236
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  • 9. Microcephaly, lymphedema, and chorioretinal dysplasia: a distinct syndrome?
    Feingold M, Bartoshesky L.
    Am J Med Genet; 1992 Aug 01; 43(6):1030-1. PubMed ID: 1415329
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  • 10. 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 Aug 01; 7(2):113-22. PubMed ID: 8831130
    [Abstract] [Full Text] [Related]

  • 11. A syndrome of multiple fundal anomalies in siblings with microcephaly without mental retardation.
    Sheriff SM, Hegab S.
    Ophthalmic Surg; 1988 May 01; 19(5):353-5. PubMed ID: 3399264
    [Abstract] [Full Text] [Related]

  • 12. The syndrome of retinal pigmentary degeneration, microcephaly, and severe mental retardation (Mirhosseini-Holmes-Walton syndrome): report of two patients.
    Mendez HM, Paskulin GA, Vallandro C.
    Am J Med Genet; 1985 Oct 01; 22(2):223-8. PubMed ID: 4050854
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  • 13. Microcephaly, lymphedema, chorioretinal dysplasia (MLCRD) syndrome.
    Kelly MN, Khuddus N, Motamarry S, Tuli S.
    J Pediatr Health Care; 2012 Oct 01; 26(4):306-11. PubMed ID: 22726716
    [No Abstract] [Full Text] [Related]

  • 14. Microcephaly and digital anomalies: a newly recognized syndrome of recessively inherited mental retardation.
    Kelly TE, Kirson L, Wyatt J.
    Am J Med Genet; 1993 Feb 01; 45(3):353-5. PubMed ID: 8434622
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  • 15. Brief clinical report: an X-linked mental retardation syndrome with craniofacial abnormalities, microcephaly and club foot.
    Holmes LB, Gang DL.
    Am J Med Genet; 1984 Jan 01; 17(1):375-82. PubMed ID: 6711605
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  • 16. Autosomal dominant microcephaly--lymphoedema-chorioretinal dysplasia syndrome.
    Casteels I, Devriendt K, Van Cleynenbreugel H, Demaerel P, De Tavernier F, Fryns JP.
    Br J Ophthalmol; 2001 Apr 01; 85(4):499-500. PubMed ID: 11302131
    [No Abstract] [Full Text] [Related]

  • 17. Alopecia, mental retardation, epilepsy and microcephaly in two cousins.
    Pridmore C, Baraitser M, Brett EM.
    Clin Dysmorphol; 1992 Apr 01; 1(2):79-84. PubMed ID: 1345516
    [Abstract] [Full Text] [Related]

  • 18. GOMBO syndrome of growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia: a possible "new" recessively inherited MCA/MR syndrome.
    Verloes A, Delfortrie J, Lambotte C.
    Am J Med Genet; 1989 Jan 01; 32(1):15-8. PubMed ID: 2705477
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