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Publications by Xiangxun Zhang
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
Related publications
Congenital Adrenal Hyperplasia Due to 11-Beta-Hydroxylase Deficiency
Correction: Congenital Adrenal Hyperplasia Due to 11-Beta-Hydroxylase Deficiency: Functional Consequences of Four CYP11B1 Mutations
European Journal of Human Genetics
Genetics
Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Steroid 21-Hydroxylase Deficiency in Mice. An Animal Model for Congenital Adrenal Hyperplasia.
Proceedings of The Japanese Association of Animal Models for Human Diseases
Psychological Vulnerability to Stress in Carriers of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Hormones
Medicine
Endocrinology
Metabolism
Diabetes
Deletion of the 21-Hydroxylase Gene in Congenital Adrenal Hyperplasia
Pediatric Research
Child Health
Pediatrics
Perinatology
Prevalence of Testicular Adrenal Rest Tumours in Male Children With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Male Gender Identity and Reversible Hypokalemic Hypertension in a 46,XX Child With 11-Beta-Hydroxylase Deficiency Congenital Adrenal Hyperplasia
Cureus
Congenital Adrenal Hyperplasia Due to Cytochrome P450 Oxidoreductase Deficiency
