Author:
Quaderi Nandita A.,Schweiger Susann,Gaudenz Karin,Franco Brunella,Rugarli Elena I.,Berger Wolfgang,Feldman George J.,Volta Manuela,Andolfi Grazia,Gilgenkrantz S.,Marion Robert W.,Hennekam Raoul C.M.,Opitz John M.,Muenke Maximilian,Ropers Hilger H.,Ballabio Andrea
Publisher
Springer Science and Business Media LLC
Reference60 articles.
1. Opitz, J.M., Summitt, R.L. & Smith, D.W. The BBB syndrome familial telecanthus with associated congenital anomalies. Birth Defects Orig. Art. Ser. (V)2, 86–94 (1969).
2. Opitz, J.M., Frias, J.L., Guttenberger, J.E. & Pellet, J.R. The G syndrome of multiple congenital anomalies. Birth Defects Orig. Art. Ser. (V)2, 95–102 (1969).
3. Opitz, J.M. G syndrome (hypertelorism with esophageal abnormality and hypospadias, or hypospadias-dysphagia, or ‘Opitz-Frias’ or ‘Opitz-G’ syndrome): perspective in 1987 and bibliography. Am. J. Med. Genet. 28, 275–285 (1987).
4. Robin, N.H., Opitz, J.M. & Muenke, M. Opitz G/BBB syndrome: clinical comparisons of families linked to Xp22 and 22q, and a review of the literature. Am. J. Med. Genet. 62, 305–317 (1996).
5. Bershof, J.F., Guyuron, B. & Olsen, M.M. G syndrome: a review of the literature and a case report. J. Craniomaxillofac. Surg. 20, 24–27 (1992).
Cited by
320 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献