文献
J-GLOBAL ID:200902221922863782
整理番号:08A0575986
HOXA2の突然変異はイラン人家族の常染色体劣性小耳症の原因になる
A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family
著者 (9件):
ALASTI Fatemeh
(Univ. Antwerp, Antwerp, BEL)
,
ALASTI Fatemeh
(National Inst. Genetic Engineering and Biotechnology, Tehran, IRN)
,
SADEGHI Abdorrahim
(National Inst. Genetic Engineering and Biotechnology, Tehran, IRN)
,
SADEGHI Abdorrahim
(Tarbiat modarres Univ., Tehran, IRN)
,
SANATI Mohammad Hossein
(National Inst. Genetic Engineering and Biotechnology, Tehran, IRN)
,
FARHADI Mohammad
(Iran Univ. Medical Sci., Tehran, IRN)
,
STOLLAR Elliot
(Hospital for Sick Children, Ontario, CAN)
,
SOMERS Thomas
(Univ. Antwerp, Antwerp, BEL)
,
VAN CAMP Guy
(Univ. Antwerp, Antwerp, BEL)
資料名:
American Journal of Human Genetics
(American Journal of Human Genetics)
巻:
82
号:
4
ページ:
982-991
発行年:
2008年04月
JST資料番号:
B0360B
ISSN:
0002-9297
資料種別:
逐次刊行物 (A)
発行国:
オランダ (NLD)
言語:
英語 (EN)