後藤治子 | 愛知県心身障害者コロニー発達障害研究所

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著作論文

赤血球型AMPデアミナーゼ完全欠損の遺伝子変異 : 稀な2変異の複合ヘテロ接合体
Lesch-Nyhan症候群におけるHPRT遺伝子変異と異常mRNAの発現
A Common Mutation in the Tyrosine Kinase Domain of the Fibroblast Growth Factor Receptor 3 Gene in Two Japanese Patients with Hypochondroplasia
Identification of Mutations in the Gene Encoding the Fibroblast Growth Factor Receptor 3 in Japanese Patients with Achondroplasia
IMP dehydrogenase in human leukemic cells
Hypoxanthine guanine phosphoribosyltransferase(HPRT)gene mutations in Korean families with Lesch-Nyhan syndrome.
Cloning of a cDNA Encoding Human Erythrocyte Type AMP Deaminase and Molecular Analysis of Mutant gene Responsible for Deficiency.
Prenatal diagnosis of HPRT mutant genes in Lesch-Nyhan syndrome

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