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51. [Dubowitz syndrome. A diagnosis not to be missed]. Mathieu M; Berquin P; Epelbaum S; Lenaerts C; Piussan C Arch Fr Pediatr; 1991 Dec; 48(10):715-8. PubMed ID: 1793348 [TBL] [Abstract][Full Text] [Related]
52. Varadi syndrome or Opitz trigonocephaly: overlapping manifestation in two cousins. Bankier A; Rose CM Am J Med Genet; 1994 Oct; 53(1):85-8. PubMed ID: 7802045 [No Abstract] [Full Text] [Related]
53. Changing phenotype in Floating-Harbor syndrome. Hersh JH; Groom KR; Yen FF; Verdi GD Am J Med Genet; 1998 Feb; 76(1):58-61. PubMed ID: 9508066 [TBL] [Abstract][Full Text] [Related]
56. Smith-Lemli-Opitz syndrome: two further cases. Gill DG; Blair AL Ir Med J; 1975 Jan; 68(2):33-6. PubMed ID: 1110157 [No Abstract] [Full Text] [Related]
57. Clinical and genetic aspects of trigonocephaly: a study of 25 cases. Azimi C; Kennedy SJ; Chitayat D; Chakraborty P; Clarke JT; Forrest C; Teebi AS Am J Med Genet A; 2003 Mar; 117A(2):127-35. PubMed ID: 12567409 [TBL] [Abstract][Full Text] [Related]
58. [Early the larche and hyperprolactinemia in the Smith-Lemli-Opitz syndrome]. Calvani M; Tirasacchi V; Toscano V; Bellussi A; Fortuna C Minerva Pediatr; 1979 Dec; 31(23):1721-32. PubMed ID: 554964 [No Abstract] [Full Text] [Related]
59. Brief clinical observations: the Neu-Laxova syndrome--a distinct entity. Lazjuk GI; Lurie IW; Ostrowskaja TI; Cherstvoy ED; Kirillova IA; Nedzved MK; Usoev SS Am J Med Genet; 1979; 3(3):261-7. PubMed ID: 225952 [TBL] [Abstract][Full Text] [Related]