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5. Chorio-retinal dysplasia, microcephaly and mental retardation. An autosomal dominant syndrome. Tenconi R; Clementi M; Moschini GB; Casara G; Baccichetti C Clin Genet; 1981 Nov; 20(5):347-51. PubMed ID: 7333029 [No Abstract] [Full Text] [Related]
6. 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]
7. 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]
8. A case of exudative vitreoretinopathy and chorioretinal coloboma associated with microcephaly in a female with contiguous Xp11.3-11.4 deletion. Hinds AM; Rosser E; Reddy MA Ophthalmic Genet; 2018 Jun; 39(3):396-398. PubMed ID: 29617172 [TBL] [Abstract][Full Text] [Related]
9. [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]
10. Chorioretinopathy with hereditary microcephaly. McKusick VA; Stauffer M; Knox DL; Clark DB Arch Ophthalmol; 1966 May; 75(5):597-600. PubMed ID: 5936364 [No Abstract] [Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. 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]
15. 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]
16. [Familial microcephaly with spasticity and epilepsy in 2 sisters]. Lesný I; Seemanová E Cesk Neurol Neurochir; 1987 Mar; 50(2):135-8. PubMed ID: 3581247 [No Abstract] [Full Text] [Related]
17. Ocular abnormalities of a child associated with familial microcephaly. Fisch RO; Ketterling WC; Schacht LE; Letson RD Am J Ophthalmol; 1973 Aug; 76(2):260-4. PubMed ID: 4199005 [No Abstract] [Full Text] [Related]
18. Ophthalmologic abnormalities in Mowat-Wilson syndrome and a mutation in ZEB2. Ariss M; Natan K; Friedman N; Traboulsi EI Ophthalmic Genet; 2012 Sep; 33(3):159-60. PubMed ID: 22486326 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Ocular abnormalities of true microcephaly. Alzial C; Dufier JL; Aicardi J; de Grouchy J; Saraux H Ophthalmologica; 1980; 180(6):333-9. PubMed ID: 6777726 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]