[HTML][HTML] Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
TM Espinosa Reyes, T Collazo Mesa… - BMC Endocrine …, 2020 - Springer
Background Congenital adrenal hyperplasia (CAH) is an autosomal recessive group of
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
[HTML][HTML] Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
TM Espinosa Reyes… - BMC …, 2020 - bmcendocrdisord.biomedcentral …
Congenital adrenal hyperplasia (CAH) is an autosomal recessive group of diseases. 21-
Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH cases. To …
Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH cases. To …
[PDF][PDF] Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
TME Reyes, TC Mesa, PAL Cruz, AA Machado… - 2020 - academia.edu
Background: Congenital adrenal hyperplasia (CAH) is an autosomal recessive group of
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
[PDF][PDF] Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
TME Reyes, TC Mesa, PAL Cruz, AA Machado… - 2020 - researchgate.net
Background: Congenital adrenal hyperplasia (CAH) is an autosomal recessive group of
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
TM Espinosa Reyes, T Collazo Mesa… - BMC Endocrine …, 2020 - search.ebscohost.com
Background: Congenital adrenal hyperplasia (CAH) is an autosomal recessive group of
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
TME Reyes, TC Mesa, PAL Cruz… - BMC endocrine …, 2020 - pubmed.ncbi.nlm.nih.gov
Background Congenital adrenal hyperplasia (CAH) is an autosomal recessive group of
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
[PDF][PDF] Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
TME Reyes, TC Mesa, PAL Cruz, AA Machado… - 2020 - scholar.archive.org
Background: Congenital adrenal hyperplasia (CAH) is an autosomal recessive group of
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
E Reyes, L Cruz, H Falhammar - BMC Endocrine Disorders, 2020 - europepmc.org
Background Congenital adrenal hyperplasia (CAH) is an autosomal recessive group of
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
TME Reyes, TC Mesa, PAL Cruz… - BMC Endocrine …, 2020 - search.proquest.com
Background Congenital adrenal hyperplasia (CAH) is an autosomal recessive group of
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
TME Reyes, TC Mesa, PAL Cruz, AA Machado… - BMC Endocrine …, 2020 - go.gale.com
Background Congenital adrenal hyperplasia (CAH) is an autosomal recessive group of
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …
diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH …