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28. Premaxillary agenesis, ocular hypotelorism holoprosencephaly, and extracranial anomalies in an infant with a normal karyogram. Rowlatt U; Pruzansky S Cleft Palate J; 1980 Jul; 17(3):197-204. PubMed ID: 6930994 [TBL] [Abstract][Full Text] [Related]
29. Agnathia-holoprosencephaly: a developmental field complex involving face and brain. Report of 3 cases. Bixler D; Ward R; Gale DD J Craniofac Genet Dev Biol Suppl; 1985; 1():241-9. PubMed ID: 3932506 [TBL] [Abstract][Full Text] [Related]
30. "Holoprosencephaly-polydactyly" (pseudotrisomy 13) syndrome: expansion of the phenotypic spectrum. Lurie IW; Wulfsberg EA Am J Med Genet; 1993 Sep; 47(3):405-9. PubMed ID: 8135289 [TBL] [Abstract][Full Text] [Related]
31. Dermatoglyphics in children suffering from congenital defects, with and without chromosomal aberrations. Usoev SS Sov Genet; 1974 Jul; 8(7):929-31. PubMed ID: 4278489 [No Abstract] [Full Text] [Related]
32. The XK-aprosencephaly syndrome. Lurie IW; Nedzed MK; Lazjuk GI; Kirillova IA; Cherstvoy ED; Ostrovskaja TI; Shved IA Am J Med Genet; 1980; 7(2):231-4. PubMed ID: 7193413 [No Abstract] [Full Text] [Related]
33. Case report: two patients with oculocerebrocutaneous syndrome and terminal digital amputations. Asher NG; Olney AH; Schaefer GB Semin Pediatr Neurol; 2008 Dec; 15(4):221-3. PubMed ID: 19073332 [TBL] [Abstract][Full Text] [Related]
34. Brief clinical report: HARD (+/- E) syndrome: report of a sixth family with support for autosomal-recessive inheritance. Aymé S; Mattei JF Am J Med Genet; 1983 Apr; 14(4):759-66. PubMed ID: 6405616 [TBL] [Abstract][Full Text] [Related]
35. Malformations and leukemia in children with Down's syndrome. Fabia J; Drolette M Pediatrics; 1970 Jan; 45(1):60-70. PubMed ID: 4243491 [No Abstract] [Full Text] [Related]
36. Double aneuploidy: 46,X, +21 a combination of Down syndrome and Turner syndrome. Ruangdaraganon N; Kotchabhakdi N; Mekanandha V J Med Assoc Thai; 1993 Oct; 76 Suppl 2():215-7. PubMed ID: 7822996 [No Abstract] [Full Text] [Related]
37. [The state of the eye in children with Down syndrome caused by trisomy 21 translocation]. Grałek M; Jakubowski L Klin Oczna; 1995 Jun; 97(6):164-6. PubMed ID: 7643555 [TBL] [Abstract][Full Text] [Related]
38. Holoprosencephaly associated with caudal dysgenesis: a clinical-epidemiological analysis. Martínez-Frías ML; Bermejo E; García A; Galán E; Prieto L Am J Med Genet; 1994 Oct; 53(1):46-51. PubMed ID: 7802035 [TBL] [Abstract][Full Text] [Related]
39. Familial Down's syndrome. Maximilian C; Pop T; Duca D; Simionescu L; Danielescu M; Ioan D Endocrinologie; 1981; 19(1):65-8. PubMed ID: 6457382 [TBL] [Abstract][Full Text] [Related]
40. Agnathia-holoprosencephaly: a midline malformation association. Hennekam RC Am J Med Genet; 1990 Aug; 36(4):525. PubMed ID: 2389812 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]