文献
J-GLOBAL ID:201902276789098669
整理番号:19A1250408
稀な頭蓋顔面特徴を伴う基底細胞母斑症候群における新規PTCH1変異
A novel PTCH1 mutation in basal cell nevus syndrome with rare craniofacial features
著者 (15件):
MURATA Yuka
(Osaka Univ. Graduate School of Dentistry, Suita, JPN)
,
KUROSAKA Hiroshi
(Osaka Univ. Graduate School of Dentistry, Suita, JPN)
,
OHATA Yasuhisa
(Osaka Univ. Graduate School of Dentistry, Suita, JPN)
,
OHATA Yasuhisa
(Osaka Univ. Graduate School of Medicine, Suita, JPN)
,
AIKAWA Tomonao
(Osaka Univ. Graduate School of Dentistry, Suita, JPN)
,
TAKAHATA Sosuke
(Osaka Univ. Graduate School of Dentistry, Suita, JPN)
,
FUJII Katsunori
(Chiba Univ., Chiba, JPN)
,
MIYASHITA Toshiyuki
(Kitasato Univ. Graduate School of Medical Sci., Sagamihara, JPN)
,
MORITA Chisato
(Osaka Univ. Graduate School of Dentistry, Suita, JPN)
,
INUBUSHI Toshihiro
(Osaka Univ. Graduate School of Dentistry, Suita, JPN)
,
KUBOTA Takuo
(Osaka Univ. Graduate School of Medicine, Suita, JPN)
,
SAKAI Norio
(Osaka Univ. Graduate School of Medicine, Suita, JPN)
,
OZONO Keiichi
(Osaka Univ. Graduate School of Medicine, Suita, JPN)
,
KOGO Mikihiko
(Osaka Univ. Graduate School of Dentistry, Suita, JPN)
,
YAMASHIRO Takashi
(Osaka Univ. Graduate School of Dentistry, Suita, JPN)
資料名:
Human Genome Variation (Web)
(Human Genome Variation (Web))
巻:
6
号:
Apr
ページ:
WEB ONLY
発行年:
2019年04月
JST資料番号:
U1014A
ISSN:
2054-345X
資料種別:
逐次刊行物 (A)
記事区分:
短報
発行国:
ドイツ (DEU)
言語:
英語 (EN)