Hypertelorism-Hypospadias Syndrome
Author:
Affiliation:
1. From the Departments of Urology and Pediatrics, Divisions of Pediatric Urology and Medical Genetics, LeBonheur Children’s Medical Center and University of Tennessee Center for Health Sciences, Memphis, Tennessee
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Urology
Reference10 articles.
1. Familial telecanthus with associated congenital anomalies;Christian;Birth Defects, Original Article Series,1969
2. The BBB syndrome—familial telecanthus with associated congenital anomalies;Opitz;Birth Defects, Original Article Series,1969
3. Studies of malformation syndromes of man VB: the hypertelorism-hypospadias (BBB) syndrome. Case report and review;Gonzalez;Eur. J. Ped.,1977
4. The hypertelorism-hypospadias syndrome;Reed;J. Canad. Ass. Rad.,1975
5. The G and BBB syndromes: case presentations, genetics and nosology;Funderburk;Amer. J. Med. Genet.,1978
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1. Craniofacial anomalies associated with hypospadias. Description of a hospital based population in South America;International braz j urol;2016-08
2. THE DIAGNOSIS AND MEDICAL MANAGEMENT OF PRIMARY VESICOURETERAL REFLUX;Pediatric Urology;2010
3. A Novel Case of Hypertelorism, Hypospadias, Strabismus, and Bilateral Congenital Lacrimal Fistulae;Journal of Pediatric Ophthalmology & Strabismus;2002-09
4. Hypospadias-hypertelorism syndrome;The Indian Journal of Pediatrics;2000-12
5. Further delineation of the Opitz G/BBB syndrome: Report of an infant with complex congenital heart disease and bladder exstrophy, and review of the literature;American Journal of Medical Genetics;1998-07-07
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