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65. "Disorganization" gene in mutations. Winter RM; Donnai D Am J Med Genet; 1990 Nov; 37(3):435-6. PubMed ID: 2260581 [No Abstract] [Full Text] [Related]
66. Opitz trigonocephaly (C)-like syndrome, or Bohring-Opitz syndrome: another example. Nakane T; Kubota T; Fukushima Y; Hata Y; Ishii J; Komiyama A Am J Med Genet; 2000 Jun; 92(5):361-2. PubMed ID: 10861668 [No Abstract] [Full Text] [Related]
67. Two-hit model for sporadic congenital anomalies in mice with the disorganization mutation. Crosby JL; Varnum DS; Nadeau JH Am J Hum Genet; 1993 May; 52(5):866-74. PubMed ID: 8488837 [TBL] [Abstract][Full Text] [Related]
68. [Case of multiple abnormalities associated with a defect of the frontal bone]. Hirota K; Sanaka M; Kotoyori Y; Ando M; Okumura T Nihon Ika Daigaku Zasshi; 1969; 36(2):182-7. PubMed ID: 5821565 [No Abstract] [Full Text] [Related]
72. Mortality, pathological findings and causes of death in the de Lange syndrome. Beck B; Fenger K Acta Paediatr Scand; 1985 Sep; 74(5):765-9. PubMed ID: 4050424 [TBL] [Abstract][Full Text] [Related]
73. Elejalde syndrome: a case report. Thornton CM; Stewart F Am J Med Genet; 1997 Apr; 69(4):406-8. PubMed ID: 9098491 [TBL] [Abstract][Full Text] [Related]
74. Opitz trigonocephaly syndrome presenting with sudden unexplained death in the operating room: a case report. Travan L; Pecile V; Fertz M; Fabretto A; Brovedani P; Demarini S; Opitz JM J Med Case Rep; 2011 Jun; 5():222. PubMed ID: 21689463 [TBL] [Abstract][Full Text] [Related]
75. [Syndrome due to anomalous styloid process]. CALICETI G; MANARA E; CASTELLINI G Otorinolaringol Ital; 1958; 26(2):118-28. PubMed ID: 13553505 [No Abstract] [Full Text] [Related]
76. [Delayed metopism as an anatomico-radiological and clinical entity]. CASSONE R Friuli Med; 1956; 11(6):909-20. PubMed ID: 13397650 [No Abstract] [Full Text] [Related]
77. Mutations in CD96, a member of the immunoglobulin superfamily, cause a form of the C (Opitz trigonocephaly) syndrome. Kaname T; Yanagi K; Chinen Y; Makita Y; Okamoto N; Maehara H; Owan I; Kanaya F; Kubota Y; Oike Y; Yamamoto T; Kurosawa K; Fukushima Y; Bohring A; Opitz JM; Yoshiura K; Niikawa N; Naritomi K Am J Hum Genet; 2007 Oct; 81(4):835-41. PubMed ID: 17847009 [TBL] [Abstract][Full Text] [Related]
78. A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C Syndrome. Urreizti R; Damanti S; Esteve C; Franco-Valls H; Castilla-Vallmanya L; Tonda R; Cormand B; Vilageliu L; Opitz JM; Neri G; Grinberg D; Balcells S Sci Rep; 2018 Jan; 8(1):694. PubMed ID: 29330474 [TBL] [Abstract][Full Text] [Related]
79. A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C Syndromes. Urreizti R; Cueto-Gonzalez AM; Franco-Valls H; Mort-Farre S; Roca-Ayats N; Ponomarenko J; Cozzuto L; Company C; Bosio M; Ossowski S; Montfort M; Hecht J; Tizzano EF; Cormand B; Vilageliu L; Opitz JM; Neri G; Grinberg D; Balcells S Sci Rep; 2017 Mar; 7():44138. PubMed ID: 28281571 [TBL] [Abstract][Full Text] [Related]