These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 7977454)

  • 1. Chorioretinal dysplasia-microcephaly-mental retardation syndrome.
    Warburg M; Heuer HE
    Am J Med Genet; 1994 Aug; 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; 226(4):344-6. PubMed ID: 19384796
    [TBL] [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; 31(2):89-93. PubMed ID: 20450312
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 53(2):99-101. PubMed ID: 7856652
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chorioretinal dysplasia-microcephaly-mental retardation syndrome: report of an American family.
    Sadler LS; Robinson LK
    Am J Med Genet; 1993 Aug; 47(1):65-8. PubMed ID: 8368255
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 86(3):215-8. PubMed ID: 10482868
    [TBL] [Abstract][Full Text] [Related]  

  • 7. On the nosology of the "primary true microcephaly, chorioretinal dysplasia, lymphoedema" association.
    Fryns JP; Smeets E; Van den Berghe H
    Clin Genet; 1995 Sep; 48(3):131-3. PubMed ID: 8556819
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Hereditary microcephaly with autosomal dominant chorioretinal dysplasia (author's transl)].
    Alzial C; Dufier JL; Brasnu C; Aicardi J; de Grouchy J
    Sem Hop; 1981 Jan 8-15; 57(1-2):43-6. PubMed ID: 6258236
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Microcephaly, lymphedema, and chorioretinal dysplasia: a distinct syndrome?
    Feingold M; Bartoshesky L
    Am J Med Genet; 1992 Aug; 43(6):1030-1. PubMed ID: 1415329
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 7(2):113-22. PubMed ID: 8831130
    [TBL] [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; 19(5):353-5. PubMed ID: 3399264
    [TBL] [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; 22(2):223-8. PubMed ID: 4050854
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Microcephaly, lymphedema, chorioretinal dysplasia (MLCRD) syndrome.
    Kelly MN; Khuddus N; Motamarry S; Tuli S
    J Pediatr Health Care; 2012; 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; 45(3):353-5. PubMed ID: 8434622
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 17(1):375-82. PubMed ID: 6711605
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 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; 1(2):79-84. PubMed ID: 1345516
    [TBL] [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; 32(1):15-8. PubMed ID: 2705477
    [No Abstract]   [Full Text] [Related]  

  • 19. ["True" microcephaly with dominant-inheritance chorioretinal dysplasia].
    Alzial C; Dufier JL; Brasnu C; Aicardi J; de Grouchy J
    Ann Genet; 1980; 23(2):91-4. PubMed ID: 6967291
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A syndrome of microcephaly, eye anomalies, short stature, and mental deficiency.
    Bouwes Bavinck JN; Weaver DD; Ellis FD; Ward RE
    Am J Med Genet; 1987 Apr; 26(4):825-31. PubMed ID: 3109242
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.