Hishinuma A | Department Of Clinical Laboratory Medicine Dokkyo University School Of Medicine
スポンサーリンク
概要
関連著者
-
Hishinuma A
Department Of Clinical Laboratory Medicine Dokkyo University School Of Medicine
-
Harada S
Department Of Mechanical Engineering Kyushu Institute Of Technology
-
Kotani T
Department Of Laboratory Medicine And Institute Of Clinical Investigation Miyazaki Medical College
-
Umeki K
Department of Laboratory Medicine and Institute of Clinical Investigation, Miyazaki Medical College
-
Umeki K
Department Of Laboratory Medicine And Institute Of Clinical Investigation Miyazaki Medical College
-
Endo F
Department Of Pediatrics Kumamoto University School Of Medicine
-
Nakamura K
Department Of Agricultural Chemistry The University Of Tokyo:(present Office)department Of Biologica
-
Tajima T
Department Of Biological Science Faculty Of Science Kumamoto University
-
Tajiri H
Department Of Pediatrics Osaka Prefecture General Hospital
-
Ieiri T
Department Of Clinical Pathology Dokkyo University School Of Medicine
-
Nishiyama S
Department Of Chemistry Keio University
-
Hishinuma A
Department of Clinical Pathology, Dokkyo University School of Medicine
-
Hishinuma A
Department Of Pediatrics Kumamoto University School Of Medicine:department Of Clinical Laboratory Me
-
Hishinuma A
Department Of Clinical Pathology Dokkyo University School Of Medicine
-
Muto Y
Department of Pediatrics, Kumamoto University, School of Medicine
-
Muto Y
Department Of Pediatrics Kumamoto University School Of Medicine:department Of Clinical Laboratory Me
-
Tajiri H
Department Of Pediatrics Kumamoto University School Of Medicine:department Of Clinical Laboratory Me
-
Endo F
Department Of Pediatrics Kumamoto University
著作論文
- 183 Two siblings with congenital goitrous hypothyroidism who were suspected to have thyroglobulin synthesis defects
- 184 COMPOUND HETEROZYGOTE IN THYROGLOBULIN GENE IN SIBLINGS OF CONGENITAL HYPOTHYROIDISM
- 45 THREE SIBLINGS WITH CONGENITAL HYPOTHYROIDISM DUE TO PARTIAL IODINE ORGANIFICATION DEFECT NOT DETECTED BY NEONATAL SCREENING
- 84 A NOVEL MUTATION OF THE THYROID PEROXIDASE GENE CAUSING PARTIAL IODIDE ORGANIFICATION DEFECT IN THREE SIBLINGS