文献
J-GLOBAL ID:201702245377793867
整理番号:17A0285076
偽副甲状腺機能低下症Ib型及びBeckwith-Wiedemann症候群の両方の臨床表現型を表す患者における多遺伝子座メチル化欠損
Multilocus methylation defects in a patient presenting with both clinical phenotype of pseudohypoparathyroidism type Ib and Beckwith-Wiedemann syndrome
著者 (9件):
SANO Shinichiro
(National Res. Inst. for Child Health and Dev., JPN)
,
MATSUBARA Keiko
(National Res. Inst. for Child Health and Dev., JPN)
,
NAGASAKI Keisuke
(Niigata Univ. Graduate School of Medical and Dental Sci., Niigata)
,
NAKAMURA Akie
(National Res. Inst. for Child Health and Dev., JPN)
,
NAKABAYASHI Kazuhiro
(National Res. Inst. for Child Health and Dev., Tokyo)
,
HATA Kenichiro
(National Res. Inst. for Child Health and Dev., Tokyo)
,
FUKAMI Maki
(National Res. Inst. for Child Health and Dev., JPN)
,
OGATA Tsutomu
(Hamamatsu Univ. School of Medicine, Hamamatsu)
,
KAGAMI Masayo
(National Res. Inst. for Child Health and Dev., JPN)
資料名:
日本人類遺伝学会大会プログラム・抄録集
(日本人類遺伝学会大会)
巻:
61st(Web)
ページ:
ROMBUNNO.Tue(3)-P-250 (WEB ONLY)
発行年:
2016年
JST資料番号:
L1204A
資料種別:
会議録 (C)
記事区分:
短報
発行国:
日本 (JPN)
言語:
英語 (EN)