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Publications by Shuichi Yatsuga

A Case of Combined 21‐hydroxylase Deficiency and CHARGE Syndrome Featuring Micropenis and Cryptorchidism

Molecular genetics & genomic medicine

Molecular Biology

English

Developmental Delay and Failure to Thrive in a 7-Month-Old Baby Boy With Spontaneous Transient Graves’ Thyrotoxicosis: A Case Report

Journal of Medical Case Reports

English

Related publications

Molecular Pathology of 21-Hydroxylase Deficiency

Pediatric Research

English

Dna Hybridization Analysis of 21-Hydroxylase Deficiency

Pediatric Research

English

HLA Class I-, Complement C4- And 21-Hydroxylase Probes in the Genetic Analysis of 21-Hydroxylase Deficiency

Clinical Chemistry and Laboratory Medicine

Clinical Biochemistry

English

Genetics and Biochemical Variability of Variants of 21 Hydroxylase Deficiency.

Journal of Medical Genetics

English

Analysis of Steroid 21-Hydroxylase Gene in Five Unrelated Japanese Patients With 21-Hydroxylase Deficiency

Endocrinologia Japonica

English

Location of the Gene for 21-Hydroxylase Deficiency

Pediatric Research

English

21-Hydroxylase Deficiency Families With HLA Identical Affected and Unaffected Sibs.

Journal of Medical Genetics

English

Clinical Course of Patients With Nonclassical 21-Hydroxylase Deficiency (21-Ohd) Diagnosed in Infancy and Childhood

Endocrine Journal

English

Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

English