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4. Holoprosencephaly: epidemiologic and clinical characteristics of a California population. Croen LA; Shaw GM; Lammer EJ Am J Med Genet; 1996 Aug; 64(3):465-72. PubMed ID: 8862623 [TBL] [Abstract][Full Text] [Related]
6. Recurrence of holoprosencephaly in families with a positive history. Benke PJ; Cohen MM Clin Genet; 1983 Nov; 24(5):324-8. PubMed ID: 6652942 [TBL] [Abstract][Full Text] [Related]
7. Microcephaly in familial holoprosencephaly. Ardinger HH; Bartley JA J Craniofac Genet Dev Biol; 1988; 8(1):53-61. PubMed ID: 3209679 [TBL] [Abstract][Full Text] [Related]
8. Trisomy 13 in two infants with cyclops. Fujimoto A; Ebbin AJ; Towner JW; Wilson MG J Med Genet; 1973 Sep; 10(3):294-6. PubMed ID: 4204339 [TBL] [Abstract][Full Text] [Related]
9. Holoprosencephaly: examples of clinical variability and etiologic heterogeneity. Corsello G; Buttitta P; Cammarata M; Lo Presti A; Maresi E; Zumpani L; Giuffrè L Am J Med Genet; 1990 Oct; 37(2):244-9. PubMed ID: 2147361 [TBL] [Abstract][Full Text] [Related]
10. Natural history of trisomy 18 and trisomy 13: I. Growth, physical assessment, medical histories, survival, and recurrence risk. Baty BJ; Blackburn BL; Carey JC Am J Med Genet; 1994 Jan; 49(2):175-88. PubMed ID: 8116665 [TBL] [Abstract][Full Text] [Related]
11. Trisomy 18 and cyclopia. Lang AF; Schlager FM; Gardner HA Teratology; 1976 Oct; 14(2):195-203. PubMed ID: 982315 [TBL] [Abstract][Full Text] [Related]
12. Segregation analysis in nonsyndromic holoprosencephaly. Odent S; Le Marec B; Munnich A; Le Merrer M; Bonaïti-Pellié C Am J Med Genet; 1998 May; 77(2):139-43. PubMed ID: 9605287 [TBL] [Abstract][Full Text] [Related]
13. Trisomy of the short arm of chromosome 4: the changing phenotype with age. Kleczkowska A; Fryns JP; van den Berghe H Ann Genet; 1992; 35(4):217-23. PubMed ID: 1296518 [TBL] [Abstract][Full Text] [Related]
14. [An analysis of the role of etiologic factors in clinically undifferentiated forms of oligophrenia]. Marincheva GS; Stonova NS; Maksimal'do IuB Zh Nevropatol Psikhiatr Im S S Korsakova; 1974; 74(10):1564-9. PubMed ID: 4473879 [No Abstract] [Full Text] [Related]
15. Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality--a new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs. Verloes A; Dodinval P; Beco L; Bonnivert J; Lambotte C Am J Med Genet; 1990 Sep; 37(1):119-23. PubMed ID: 2240028 [TBL] [Abstract][Full Text] [Related]
16. The risk of having a second retarded child. Costeff H; Weller L Am J Med Genet; 1987 Aug; 27(4):753-66. PubMed ID: 3321988 [TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia. Chen CP; Devriendt K; Lee CC; Chen WL; Wang W; Wang TY Prenat Diagn; 1999 Oct; 19(10):986-9. PubMed ID: 10521829 [TBL] [Abstract][Full Text] [Related]
18. The 18p- syndrome. Report of five cases. Zumel RM; Darnaude MT; Delicado A; Diaz de Bustamante A; de Torres ML; López-Pájares I Ann Genet; 1989; 32(3):160-3. PubMed ID: 2817777 [TBL] [Abstract][Full Text] [Related]
19. High risk for unbalanced segregation of some reciprocal translocations: a large pedigree containing distal 4q trisomy from t(4;7)(q28;p22). Francisco-Bagnariolli AM; Payão SL; Kawasaki-Oyama RS; Sabbag Filho D; Segato R; de Labio RW; Chauffaille ML; Priest JH Am J Med Genet; 2001 Nov; 103(4):302-7. PubMed ID: 11746010 [TBL] [Abstract][Full Text] [Related]
20. [Orofaciodigital syndrome. Apropos of an 11th case in the same family]. Vissian L; Vaillaud JC Ann Dermatol Syphiligr (Paris); 1972; 99(1):5-20. PubMed ID: 5053179 [No Abstract] [Full Text] [Related] [Next] [New Search]