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Publications by Hiya Boro
Male Gender Identity and Reversible Hypokalemic Hypertension in a 46,XX Child With 11-Beta-Hydroxylase Deficiency Congenital Adrenal Hyperplasia
Cureus
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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
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Prevalence of Testicular Adrenal Rest Tumours in Male Children With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
European Journal of Endocrinology
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Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
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
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11-Beta-Hydroxylase Deficiency
Gender Reversal and Bilateral Giant Adrenal Myelolipomas in a 46,xx Patient With 21-Hydroxylase Deficiency: Case Report and Review of the Literature
AACE Clinical Case Reports
Steroid 21-Hydroxylase Deficiency in Mice. An Animal Model for Congenital Adrenal Hyperplasia.
Proceedings of The Japanese Association of Animal Models for Human Diseases
Genotype-Phenotype Correlation in 1,507 Families With Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency
Proceedings of the National Academy of Sciences of the United States of America
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