文献
J-GLOBAL ID:202002229829147354
整理番号:20A0638065
てんかんと知的障害のある女児の症例提示からの16p13.3微小欠失症候群の精密化
Refinement of 16p13.3 microdeletion syndrome from a case presentation of a girl with epilepsy and intellectual disability
著者 (5件):
Kuroda Yukiko
(Division of Medical Genetics, Kanagawa Children’s Medical Center, Yokohama, Japan)
,
Kimura Yuichi
(Clinical Research Institute, Kanagawa Children’s Medical Center, Yokohama, Japan)
,
Uehara Tomoko
(Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan)
,
Kosaki Kenjiro
(Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan)
,
Kurosawa Kenji
(Division of Medical Genetics, Kanagawa Children’s Medical Center, Yokohama, Japan)
資料名:
Congenital Anomalies (Web)
(Congenital Anomalies (Web))
巻:
60
号:
2
ページ:
75-77
発行年:
2020年
JST資料番号:
U0506A
ISSN:
1741-4520
資料種別:
逐次刊行物 (A)
記事区分:
短報
発行国:
アメリカ合衆国 (USA)
言語:
英語 (EN)