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Publications by Miyuki Kitamura

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

Molecular genetics & genomic medicine
GeneticsMolecular Biology
2019English

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
Medicine
2016English

Related publications

Molecular Pathology of 21-Hydroxylase Deficiency

Pediatric Research
Child HealthPediatricsPerinatology
1993English

Dna Hybridization Analysis of 21-Hydroxylase Deficiency

Pediatric Research
Child HealthPediatricsPerinatology
1986English

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

Clinical Chemistry and Laboratory Medicine
BiochemistryMedicineClinical Biochemistry
1990English

Genetics and Biochemical Variability of Variants of 21 Hydroxylase Deficiency.

Journal of Medical Genetics
Genetics
1985English

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

Endocrinologia Japonica
1987English

Location of the Gene for 21-Hydroxylase Deficiency

Pediatric Research
Child HealthPediatricsPerinatology
1979English

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

Journal of Medical Genetics
Genetics
1989English

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

Endocrine Journal
EndocrinologyMetabolismDiabetes
2008English

Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

2020English

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