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Lumbroso S 1
Showing records 1 to 1 | Display all abstracts from Lumbroso S9721 A novel point mutation of the androgen receptor (F804L) in an Egyptian newborn with complete androgen insensitivity associated with congenital glaucoma and hypertrophic pyloric stenosis
Gad YZ; Mazen I; Lumbroso S; Temtamy SA; Sultan C
Clinical Genetics 2003; 63: 59-63
