文献
J-GLOBAL ID:201202214181025465
整理番号:12A0515209
2q31.1微小欠損症候群: 関連臨床表現型の再定義
2q31.1 microdeletion syndrome: redefining the associated clinical phenotype
著者 (14件):
DIMITROV Boyan
(Univ. Hospitals, Leuven, BEL)
,
BALIKOVA Irina
(Univ. Hospitals, Leuven, BEL)
,
DE RAVEL Thomy
(Univ. Hospitals, Leuven, BEL)
,
VAN ESCH Hilde
(Univ. Hospitals, Leuven, BEL)
,
DE SMEDT Maryse
(Univ. Hospitals, Leuven, BEL)
,
DE SMEDT Maryse
(AZ Sint-Augustinus, Wilrijk, BEL)
,
BATEN Emiel
(Sint Lucas Hospital, Bruges, BEL)
,
VERMEESCH Joris Robert
(Univ. Hospitals, Leuven, BEL)
,
BRADINOVA Irena
(Medical Univ. Sofia, Sofia, BGR)
,
SIMEONOV Emil
(Medical Univ. Sofia, Sofia, BGR)
,
DEVRIENDT Koen
(Univ. Hospitals, Leuven, BEL)
,
FRYNS Jean-Pierre
(Univ. Hospitals, Leuven, BEL)
,
DEBEER Philippe
(Univ. Hospitals, Leuven, BEL)
,
DEBEER Philippe
(Univ. Hospitals, Pellenberg, BEL)
資料名:
Journal of Medical Genetics
(Journal of Medical Genetics)
巻:
48
号:
2
ページ:
98-104
発行年:
2011年02月
JST資料番号:
T0190A
ISSN:
0022-2593
資料種別:
逐次刊行物 (A)
発行国:
イギリス (GBR)
言語:
英語 (EN)