Congenital adrenal hyperplasia
SF Witchel, R Azziz - Journal of pediatric and adolescent gynecology, 2011 - Elsevier
Congenital adrenal hyperplasia (CAH) due to P450c21 (21-hydroxylase deficiency) is a
common autosomal recessive disorder. This disorder is due to mutations in the CYP21A2 …
common autosomal recessive disorder. This disorder is due to mutations in the CYP21A2 …
Congenital Adrenal Hyperplasia
SF Witchel, R Azziz - Journal of Pediatric and Adolescent Gynecology, 2011 - infona.pl
Congenital adrenal hyperplasia (CAH) due to P450c21 (21-hydroxylase deficiency) is a
common autosomal recessive disorder. This disorder is due to mutations in the CYP21A2 …
common autosomal recessive disorder. This disorder is due to mutations in the CYP21A2 …
Congenital adrenal hyperplasia
SF Witchel, R Azziz - Journal of pediatric and adolescent …, 2011 - pubmed.ncbi.nlm.nih.gov
Congenital adrenal hyperplasia (CAH) due to P450c21 (21-hydroxylase deficiency) is a
common autosomal recessive disorder. This disorder is due to mutations in the CYP21A2 …
common autosomal recessive disorder. This disorder is due to mutations in the CYP21A2 …
Congenital Adrenal Hyperplasia
SF Witchel, R Azziz - Journal of Pediatric and Adolescent …, 2011 - jpagonline.org
Congenital adrenal hyperplasia (CAH) due to P450c21 (21-hydroxylase deficiency) is a
common autosomal recessive disorder. This disorder is due to mutations in the CYP21A2 …
common autosomal recessive disorder. This disorder is due to mutations in the CYP21A2 …
Congenital Adrenal Hyperplasia
SF Witchel, R Azziz - Journal of Pediatric and Adolescent …, 2011 - augusta.elsevierpure.com
Congenital adrenal hyperplasia (CAH) due to P450c21 (21-hydroxylase deficiency) is a
common autosomal recessive disorder. This disorder is due to mutations in the CYP21A2 …
common autosomal recessive disorder. This disorder is due to mutations in the CYP21A2 …
Congenital adrenal hyperplasia.
SF Witchel, R Azziz - Journal of Pediatric and Adolescent …, 2011 - europepmc.org
Congenital adrenal hyperplasia (CAH) due to P450c21 (21-hydroxylase deficiency) is a
common autosomal recessive disorder. This disorder is due to mutations in the CYP21A2 …
common autosomal recessive disorder. This disorder is due to mutations in the CYP21A2 …