Chondrodysplasia, situs inversus totalis, cleft epiglottis and larynx, hexadactyly of hands and feet, pancreatic cystic dysplasia, renal dysplasia/ absence, micropenis and ambiguous genitalia, imperforate anus
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference8 articles.
1. Smith-Lemli-Opitz syndrome-type II: Multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality
2. Ellis-van Creveld Syndrome Associated with Complete Situs Inversus
3. Smith-Lemli-Opitz syndromes: Do they include the Pallister-Hall syndrome?
4. Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly—a new syndrome? Part I: Clinical, causal, and pathogenetic considerations
5. (1988): “Smith's Recognizable Patterns of Human Malformation.” 4th ed. Philadelphia: W. B. Saunders Co., p 114.
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1. Atrioventricular canal defect and associated genetic disorders: new insights into polydactyly syndromes;Cardiogenetics;2011-07-26
2. REFERENCES (GAMUTS);Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007
3. Atrioventricular canal defect in Bardet-Biedl syndrome: Clinical evidence supporting the link between atrioventricular canal defect and polydactyly syndromes with ciliary dysfunction536;Genetics in Medicine;2006-08
4. Bifid epiglottis revisited;International Journal of Pediatric Otorhinolaryngology Extra;2006-06
5. Significance of bifid epiglottis;American Journal of Medical Genetics Part A;2005
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