Molecular Variability of Cyp21/C4 Gene Organization and Cyp21B Mutations in Disease-Causing Alleles of Brazilian Families with 21-Hydroxylase Deficiency

被引：0
|
作者：
L C Paulino
M de Araujo
G Guerra
M T M Baptista
S H V L Marini
M P De Mello
机构：
[1] Centro de Biologia Molecular e Engenharia Genética,
[2] Universidade Estadual de Campinas,undefined
[3] Depto. de Pediatria,undefined
[4] Faculdade de Ciêcias Médicas,undefined
[5] Universidade Estadual de Campinas,undefined
来源：
Pediatric Research | 1999年 / 45卷
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页码：443 / 443
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