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5. Opitz BBBG syndrome: new family with late-onset, serious complication. Schrander J, Schrander-Stumpel C, Berg J, Frias JL. Clin Genet; 1995 Aug 15; 48(2):76-9. PubMed ID: 7586655 [Abstract] [Full Text] [Related]
6. Phenotypic overlap of the BBB and G syndromes. Cordero JF, Holmes LB. Am J Med Genet; 1978 Aug 15; 2(2):145-52. PubMed ID: 263434 [Abstract] [Full Text] [Related]
8. Multidisciplinary management of Opitz G BBB syndrome. Parashar SY, Anderson PJ, Cox TC, McLean N, David DJ. Ann Plast Surg; 2005 Oct 15; 55(4):402-7. PubMed ID: 16186708 [Abstract] [Full Text] [Related]
10. Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22. Quaderi NA, Schweiger S, Gaudenz K, Franco B, Rugarli EI, Berger W, Feldman GJ, Volta M, Andolfi G, Gilgenkrantz S, Marion RW, Hennekam RC, Opitz JM, Muenke M, Ropers HH, Ballabio A. Nat Genet; 1997 Nov 15; 17(3):285-91. PubMed ID: 9354791 [Abstract] [Full Text] [Related]
11. G syndrome (hypertelorism with esophageal abnormality and hypospadias, or hypospadias-dysphagia, or "Opitz-Frias" or "Opitz-G" syndrome)--perspective in 1987 and bibliography. Opitz JM. Am J Med Genet; 1987 Oct 15; 28(2):275-85. PubMed ID: 3322001 [No Abstract] [Full Text] [Related]
15. X-linked midline defects. Toriello HV, Higgins JV. Am J Med Genet; 1985 May 15; 21(1):143-6. PubMed ID: 4039891 [Abstract] [Full Text] [Related]
16. Opitz GBBB syndrome and the 22q11.2 deletion. Lacassie Y, Arriaza MI. Am J Med Genet; 1996 Mar 29; 62(3):318. PubMed ID: 8882795 [No Abstract] [Full Text] [Related]
18. Three siblings with Robert's syndrome. Zergollern L, Hitrec F. Clin Genet; 1976 Apr 29; 9(4):433-6. PubMed ID: 177235 [Abstract] [Full Text] [Related]
19. Surgical management of penoscrotal hypospadias in a child with Opitz G/BBB syndrome: a case report. Ahmed F, Altam A, Alyhari Q, Badheeb M, Aljbri W, Al-Wageeh S, Al-Naggar A, Ghabisha S, Al-Shami E. Pan Afr Med J; 2023 Apr 29; 44():103. PubMed ID: 37250678 [Abstract] [Full Text] [Related]