Ogata T | Department Of Endocrinology And Metabolism National Research Institute For Child Health And Developm

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著作論文

55 GROWTH RRESPONSE TO GROWTH HORMONE
67 THE ROLE OF KAL1 GENE AND KAL2 GENE (FGFR1) IN KALLMANN SYNDROME : MUTATION ANALYSIS AND CLINICAL ASSESSMENT IN 35 PATIENTS WITH KALLMANN SYNDROME
77 PTPN11 GENE AND NOONAN/LEOPARD SYNDROME, MUTATIONS ANALYSIS AND COMPARISIONS OF THE CLINlCAL FEATURES OF 45 JAPANESE PATIENTS
82 MATERNAL UNIPARENTAL ISODISOMY FOR CHROMOSOME 7 IN A CASE WITH SILVER-RUSSELL SYNDROME
48 TARGET HEIGHT AND TARGET RANGE FOR THE JAPANESE : REVISITED
37 WIDE PHENOTYPIC SPECTRUM OF GATA3 HAPLOINSUFFICIENCY : ANALYSIS OF 11 JAPANESE FAMILIES
29 TURNER SYNDROME AND XP DELETIONS : CLINICAL AND MOLECULAR STUDIES IN 47 PATIENTS
16 PREVALENCE OF SHOX HAPLOINSUFFICIENCY IN 900 PATIENTS WITH IDIOPATHIC SHORT STATURE
30 SHOX NULLIZYGOSITY AND HAPLOINSUFFICIENCY IN A JAPANESE FAMILY : IMPLICATION FOR THE DEVELOPMENT OF TURNER SKELETAL FEATURES.
66 URINE 5β/5α-REDUCED STEROID RATIO : INFLUENCE OF MUTAIONS AND POLYMORPHISM OF THE STEROID 5α REDUCTASE-2 GENE
155 SHOX HAPLOINSUFFICIENCY AND NORMAL OVARIAN FUNCTION VS. SHOX OVERDOSAGE AND GONADAL ESTROGEN DEFICIENCY : LONGITUDINALAUXOLOGICAL STUDY

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