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Publications by Ikuko Sato
Genetic Analysis of Two Japanese Patients With Non-Classical 21-Hydroxylase Deficiency
Internal Medicine
Internal Medicine
Medicine
Related publications
Analysis of Steroid 21-Hydroxylase Gene in Five Unrelated Japanese Patients With 21-Hydroxylase Deficiency
Endocrinologia Japonica
Genetic Analysis of Classical 21-Hydroxylase Deficiency Using Polymerase Chain Reaction and Allele-Specific Oligonucleotide Hybridization
Clinical Pediatric Endocrinology
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Perinatology
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HLA Class I-, Complement C4- And 21-Hydroxylase Probes in the Genetic Analysis of 21-Hydroxylase Deficiency
Clinical Chemistry and Laboratory Medicine
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Dna Hybridization Analysis of 21-Hydroxylase Deficiency
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HLA and Hormonal Studies in Families of Patients With 21-Hydroxylase Deficiency - Cryptic Patients?
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Molecular Pathology of 21-Hydroxylase Deficiency
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Child Health
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Clinical Course of Patients With Nonclassical 21-Hydroxylase Deficiency (21-Ohd) Diagnosed in Infancy and Childhood
Endocrine Journal
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Metabolism
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Mutation Analysis of the Phenylalanine Hydroxylase Gene and Its Clinical Implications in Two Japanese Patients With Non-Phenylketonuria Hyperphenylalaninemia
Journal of Human Genetics
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Location of the Gene for 21-Hydroxylase Deficiency
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