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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 [TBL] [Abstract][Full Text] [Related]
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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. New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation. Tsukahara M; Sugio Y J Hum Genet; 1998; 43(4):224-7. PubMed ID: 9852671 [TBL] [Abstract][Full Text] [Related]
9. Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay. Feingold M; Hall BD; Lacassie Y; Martínez-Frías ML Am J Med Genet; 1997 Mar; 69(3):245-9. PubMed ID: 9096752 [TBL] [Abstract][Full Text] [Related]
10. 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]
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]
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14. The microcephaly-lymphoedema syndrome: report of an additional family. Kozma C; Scribanu N; Gersh E Clin Dysmorphol; 1996 Jan; 5(1):49-54. PubMed ID: 8867659 [TBL] [Abstract][Full Text] [Related]
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17. 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]
19. Microcephaly-lymphedema-chorioretinal dysplasia associated with pachymicrogyria and atrophy of the cerebellar vermis: an integration of brain-ocular migration disorders. Pastora N; Peralta J; Canal-Fontcuberta I; Grabowska A; Pulido JS; Abelairas J; Armada F; Garcia-Alix A Ophthalmic Genet; 2012 Jun; 33(2):116-8. PubMed ID: 22420539 [TBL] [Abstract][Full Text] [Related]
20. Documentation of anomalies not previously described in Fryns syndrome. Arnold SR; Debich-Spicer D D; Opitz JM; Gilbert-Barness E Am J Med Genet A; 2003 Jan; 116A(2):179-82; discussion 183. PubMed ID: 12494439 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]