文献
J-GLOBAL ID:202002264820157991
整理番号:20A0976456
Schaaf-Yang症候群は乳児期にPrader-Willi症候群様表現型を示す【JST・京大機械翻訳】
Schaaf-Yang syndrome shows a Prader-Willi syndrome-like phenotype during infancy
著者 (10件):
Negishi Yutaka
(Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan)
,
Ieda Daisuke
(Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan)
,
Hori Ikumi
(Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan)
,
Nozaki Yasuyuki
(Department of Pediatrics, Jichi Medical University, Tochigi, Japan)
,
Yamagata Takanori
(Department of Pediatrics, Jichi Medical University, Tochigi, Japan)
,
Komaki Hirofumi
(Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan)
,
Tohyama Jun
(Department of Child Neurology, Nishi-Niigata Chuo National Hospital, Niigata, Japan)
,
Nagasaki Keisuke
(Division of Pediatrics, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan)
,
Tada Hiroko
(Department of Pediatrics, Chibaken Saiseikai Narashino Hospital, Narashino, Japan)
,
Saitoh Shinji
(Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan)
資料名:
Orphanet Journal of Rare Diseases (Web)
(Orphanet Journal of Rare Diseases (Web))
巻:
14
号:
1
ページ:
1-7
発行年:
2019年
JST資料番号:
U7532A
ISSN:
1750-1172
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
イギリス (GBR)
言語:
英語 (EN)