文献
J-GLOBAL ID:201102268180421222
整理番号:11A1761259
遺伝性出血性毛細管拡張症:1つの家族における2つの識別可能なENG欠失
Hereditary hemorrhagic telangiectasia: two distinct ENG deletions in one family
著者 (10件):
WOODERCHAK W
(ARUP Inst. for Clinical and Experimental Pathology, UT, USA)
,
GEDGE F
(ARUP Inst. for Clinical and Experimental Pathology, UT, USA)
,
MCDONALD M
(ARUP Inst. for Clinical and Experimental Pathology, UT, USA)
,
KRAUTSCHEID P
(ARUP Inst. for Clinical and Experimental Pathology, UT, USA)
,
WANG X
(Henry Ford Health System, MI, USA)
,
MALKIEWICZ J
(Henry Ford Health System, MI, USA)
,
BUKJIOK CJ
(ARUP Inst. for Clinical and Experimental Pathology, UT, USA)
,
LEWIS T
(ARUP Inst. for Clinical and Experimental Pathology, UT, USA)
,
BAYRAK-TOYDEMIR P
(ARUP Inst. for Clinical and Experimental Pathology, UT, USA)
,
BAYRAK-TOYDEMIR P
(Univ. of Utah, UT, USA)
資料名:
Clinical Genetics
(Clinical Genetics)
巻:
78
号:
5
ページ:
484-489
発行年:
2010年11月
JST資料番号:
E0526B
ISSN:
0009-9163
資料種別:
逐次刊行物 (A)
発行国:
アメリカ合衆国 (USA)
言語:
英語 (EN)