OGATA Tsutomu | Department of Endocrinology and Metabolism, National Research Institute for Child Health and Develop

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著作論文

Monozygotic female twins discordant for Silver-Russell syndrome and hypomethylation of the H19-DMR
Identification of novel RMRP mutations and specific founder haplotypes in Japanese patients with cartilage-hair hypoplasia
Determination of specific activities and kinetic constants of biotinidase and lipoamidase in LEW rat and Lactobacillus casei (Shirota)
Identification and characterization of cryptic SHOX intragenic deletions in three Japanese patients with Leri-Weill dyschondrosteosis
Statural Growth in 31 Japanese Patients with SHOX Haploinsufficiency : Support for a Disadvantageous Effect of Gonadal Estrogens
Kallmann Syndrome Phenotype in a Female Patient with CHARGE Syndrome and CHD7 Mutation
Association of Micropenis with Pro185Ala Polymorphism of the Gene for Aryl Hydrocarbon Receptor Repressor Involved in Dioxin Signaling
A Case of XYY Syndrome with Short Stature
Mental Retardation in A Girl with Turner's Syndrome with An Active Ring X Chromosome Missing XIST
Incidental deviation of short and long CAG repeats in the androgen receptor gene for Japanese male infertility
Growth Hormone and Gonadotropin-Releasing Hormone Analog Therapy in Haploinsufficiency of SHOX
KRAS Analysis in 34 Noonan Syndrome Patients without PTPN11 Mutation
Association of Common LH Variant with Hyperfunctional Promoter in a Japanese Infertile Woman
Target Height and Target Range for Japanese Children : Revisited
Clinical findings and P450 Oxidoreductase (POR) gene analysis in Antley-Bixler syndrome with abnormal genitalia

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