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Publications by Shuki MIZUTANI
Clinical Course of Patients With Nonclassical 21-Hydroxylase Deficiency (21-Ohd) Diagnosed in Infancy and Childhood
Endocrine Journal
Endocrinology
Metabolism
Diabetes
Related publications
Analysis of Steroid 21-Hydroxylase Gene in Five Unrelated Japanese Patients With 21-Hydroxylase Deficiency
Endocrinologia Japonica
HLA and Hormonal Studies in Families of Patients With 21-Hydroxylase Deficiency - Cryptic Patients?
Pediatric Research
Child Health
Pediatrics
Perinatology
Molecular Pathology of 21-Hydroxylase Deficiency
Pediatric Research
Child Health
Pediatrics
Perinatology
Genetic Analysis of Two Japanese Patients With Non-Classical 21-Hydroxylase Deficiency
Internal Medicine
Internal Medicine
Medicine
HLA Class I-, Complement C4- And 21-Hydroxylase Probes in the Genetic Analysis of 21-Hydroxylase Deficiency
Clinical Chemistry and Laboratory Medicine
Biochemistry
Medicine
Clinical Biochemistry
Dna Hybridization Analysis of 21-Hydroxylase Deficiency
Pediatric Research
Child Health
Pediatrics
Perinatology
Location of the Gene for 21-Hydroxylase Deficiency
Pediatric Research
Child Health
Pediatrics
Perinatology
21-Hydroxylase Deficiency Families With HLA Identical Affected and Unaffected Sibs.
Journal of Medical Genetics
Genetics
Genetics and Biochemical Variability of Variants of 21 Hydroxylase Deficiency.
Journal of Medical Genetics
Genetics