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Publications by Nathalie Meurice
Erratum To: Two Novel Mutations in CYP11B1 and Modeling the Consequent Alterations of the Translated Protein in Classic Congenital Adrenal Hyperplasia Patients
Endocrine
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Non-Classic Congenital Adrenal Hyperplasia
Steroids
Organic Chemistry
Molecular Biology
Pharmacology
Biochemistry
Endocrinology
Clinical Biochemistry
Mutations in the CYP11B1 Gene Causing Congenital Adrenal Hyperplasia and Hypertension Cluster in Exons 6, 7, and 8.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Correction: Congenital Adrenal Hyperplasia Due to 11-Beta-Hydroxylase Deficiency: Functional Consequences of Four CYP11B1 Mutations
European Journal of Human Genetics
Genetics
Functional Studies of Novel CYP21A2 Mutations Detected in Norwegian Patients With Congenital Adrenal Hyperplasia
Endocrine Connections
Internal Medicine
Endocrinology
Metabolism
Diabetes
Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Classic Congenital Adrenal Hyperplasia and Its Impact on Reproduction
Fertility and Sterility
Gynecology
Reproductive Medicine
Obstetrics
Novel Variants of CYP21A2 in Vietnamese Patients With Congenital Adrenal Hyperplasia
Molecular genetics & genomic medicine
Genetics
Molecular Biology
The Combination of a Novel 2 Bp Deletion Mutation and p.D63H in CYP11B1 Cause Congenital Adrenal Hyperplasia Due to Steroid 11β-Hydroxylase Deficiency
Endocrine Journal
Endocrinology
Metabolism
Diabetes
Severe Hirsutism in Non Classic Congenital Adrenal Hyperplasia: A Case Report and Literature Review
Open Access Macedonian Journal of Medical Sciences
Medicine
