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10. "C" trigonocephaly syndrome: report of a child with agenesis of the corpus callosum and tetralogy of Fallot, and review. Glickstein J; Karasik J; Caride DG; Marion RW Am J Med Genet; 1995 Mar; 56(2):215-8. PubMed ID: 7625448 [TBL] [Abstract][Full Text] [Related]
11. Marfanoid features and craniosynostosis: report of one case and review. Lacombe D; Battin J Clin Dysmorphol; 1993 Jul; 2(3):220-4. PubMed ID: 8287183 [TBL] [Abstract][Full Text] [Related]
12. New multiple congenital anomalies: mental retardation syndrome (MCA/MR) with facio-cutaneous-skeletal involvement. Borochowitz Z; Pavone L; Mazor G; Rizzo R; Dar H Am J Med Genet; 1992 Jul; 43(4):678-85. PubMed ID: 1621757 [TBL] [Abstract][Full Text] [Related]
13. Craniosynostosis and lid anomalies: report of a girl with Michels syndrome. Cunniff C; Jones KL Am J Med Genet; 1990 Sep; 37(1):28-30. PubMed ID: 2240039 [TBL] [Abstract][Full Text] [Related]
14. The Cohen syndrome. Fryns JP; Van den Berghe H J Genet Hum; 1981 Dec; 29(4):449-53. PubMed ID: 7328419 [TBL] [Abstract][Full Text] [Related]
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17. Heterogeneity versus variability in megalocornea-mental retardation (MMR) syndromes: report of new cases and delineation of 4 probable types. Verloes A; Journel H; Elmer C; Misson JP; Le Merrer M; Kaplan J; Van Maldergem L; Deconinck H; Meire F Am J Med Genet; 1993 Apr; 46(2):132-7. PubMed ID: 8484397 [TBL] [Abstract][Full Text] [Related]