Hasegawa Y | Tokyo Metropolitan Kiyose Children's Hospital

スポンサーリンク

概要

関連著者

もっと見る

著作論文

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
11 CAN GH TREATMENT IMPROVE THE FINAL HEIGHT OF CHILDREN WITH NON-GHD SHORT STATURE?
39 TWENTY CHILDREN WITH CUSHING SYNDROME (CS) TREATED IN EIGHT MEDICAL CENTRES
90 MUTATION ANALYSIS IN A JAPANESE KIDRED WITH SPONDYLOEPIPHYSEAL DYSPLASIA TARDA
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
66 URINE 5β/5α-REDUCED STEROID RATIO : INFLUENCE OF MUTAIONS AND POLYMORPHISM OF THE STEROID 5α REDUCTASE-2 GENE

スポンサーリンク