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1 ANALYSIS OF POINT MUTATIONS (PM) OF CYP 21B GENE IN PATIENTS WITH 21-HYDROXYLASE DEFICIENCY (CAH)
Dardis, A, Saracco, N, Rivarola, M A, Belgorosky, AVolume:
36
Language:
english
Journal:
Pediatric Research
DOI:
10.1203/00006450-199411000-00059
Date:
November, 1994
File:
PDF, 98 KB
english, 1994