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Vanishing testis
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MYRFハプロ不全は性分化疾患の46,XYおよび46,XX異常を引き起こす
2019
hamanaka kouhei
takada atusi
utiyama yuri
miyatake satoko
miyake kiko
mituhasi satomi
nakazima kousi
mizuguti tuyosi
sai tu hirotomo
wada yuka
minami sawako
fukui yuu ko
masunaga youhei
fukami maki
hasegawa hou en
ogata tutomu
matumoto tyokutuu
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NR5A1は,46,XX精巣性性分化疾患の新規発症責任遺伝子である
2016
igarasi maki
takazawa kei
hakoda akiko
kanno junko
takada syuuzi
inui masasi
miyako mami
fukui yuu ko
narumi satosi
baba suu
morohasi ken'itirou
tazima tosihiro
sin ken'itirou
nakabayasi kazuhiko
matubara youiti
sekido ryouhei
ogata tutomu
kasima ta ken'iti
fukami maki
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性分化・性成熟疾患群における診療ガイドラインの作成と普及に関する研究 ガイドライン作成に必要とされる遺伝子診断および症例登録・検体保存
2016
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igarasi maki
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Vanishing Testis SyndromeにおけるDSD関連遺伝子の網羅的変異解析
2015
The Japanese Society for Pediatric Endocrinology
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フィーダー細胞を必要としないES細胞株(E14TG2a)を用いたキメラマウスの作成
1998
suzuki ri ka
nakahara youko
motegi yosiko
fukui yuu ko
yokoyama mine suke
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