Unusual case of Smith-Lemli-Opitz syndrome “type II”
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference14 articles.
1. Female external genitalia and müllerian duct derivatives in a 46,XY infant with the Smith-Lemli-Opitz syndrome
2. Smith-Lemli-Opitz syndrome-type II: Multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality
3. The lethal multiple congenital anomaly syndrome of polydactyly, sex reversal, renal hypoplasia, and unilobular lungs.
4. Defective cholesterol biosynthesis in Smith-Lemli-Opitz syndrome
5. The mis-expression of posterior Hox-4 genes in talpid (ta3) mutant wings correlates with the absence of anteroposterior polarity
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