Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Lars Breivik
Functional Studies of Novel CYP21A2 Mutations Detected in Norwegian Patients With Congenital Adrenal Hyperplasia
Endocrine Connections
Internal Medicine
Endocrinology
Metabolism
Diabetes
Related publications
Novel Variants of CYP21A2 in Vietnamese Patients With Congenital Adrenal Hyperplasia
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Complement Component 4 Copy Number Variation and CYP21A2 Genotype Associations in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Human Genetics
Genetics
Nonclassic Congenital Adrenal Hyperplasia
Current Opinion in Endocrinology, Diabetes and Obesity
Internal Medicine
Nutrition
Endocrinology
Dietetics
Medicine
Metabolism
Diabetes
Letter: Congenital Adrenal Hyperplasia.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Correction: Congenital Adrenal Hyperplasia Due to 11-Beta-Hydroxylase Deficiency: Functional Consequences of Four CYP11B1 Mutations
European Journal of Human Genetics
Genetics
Parental Management of Adrenal Crisis in Children With Congenital Adrenal Hyperplasia
Journal for specialists in pediatric nursing : JSPN
Pediatrics
Erratum To: Two Novel Mutations in CYP11B1 and Modeling the Consequent Alterations of the Translated Protein in Classic Congenital Adrenal Hyperplasia Patients
Endocrine
Non-Classic Congenital Adrenal Hyperplasia
Steroids
Organic Chemistry
Molecular Biology
Pharmacology
Biochemistry
Endocrinology
Clinical Biochemistry
Bone Mineral Status in Children With Congenital Adrenal Hyperplasia
Journal of Pediatric Endocrinology and Metabolism
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
