文献
J-GLOBAL ID:201802217396157323
整理番号:18A1006075
ヒアリン線維腫症症候群を有する大レバノン族における全ゲノム配列決定の診断的意義【JST・京大機械翻訳】
Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome
著者 (13件):
Haidar Zahraa
(Unite de Genetique Medicale, Faculte de Medecine, Universite Saint-Joseph, Beirut, Lebanon)
,
Temanni Ramzi
(Bioinformatics Division, Sidra Medical & Research Center, Doha, Qatar)
,
Chouery Eliane
(Unite de Genetique Medicale, Faculte de Medecine, Universite Saint-Joseph, Beirut, Lebanon)
,
Jithesh Puthen
(Bioinformatics Division, Sidra Medical & Research Center, Doha, Qatar)
,
Liu Wei
(Genomics Core Laboratory, Translational Medicine Division, Sidra Medical & Research Center, Doha, Qatar)
,
Al-Ali Rashid
(Bioinformatics Division, Sidra Medical & Research Center, Doha, Qatar)
,
Wang Ena
(Genomics Core Laboratory, Translational Medicine Division, Sidra Medical & Research Center, Doha, Qatar)
,
Marincola Francesco M
(Research office, Sidra Medical & Research Center, Doha, Qatar)
,
Jalkh Nadine
(Unite de Genetique Medicale, Faculte de Medecine, Universite Saint-Joseph, Beirut, Lebanon)
,
Haddad Soha
(Department of Radiology, Hotel Dieu de France University hospital-Beirut, Beirut, Lebanon)
,
Haidar Wassim
(Department of General surgery, Dar Al Amal University Hospital-Baalbeck, Baalbeck, Lebanon)
,
Chouchane Lotfi
(Laboratory of Genetic Medicine and Immunology, Weill Cornell Medicine-Qatar, Doha, Qatar)
,
Megarbane Andre
(Institut Jerome Lejeune, Paris, France)
資料名:
BMC Genetics (Web)
(BMC Genetics (Web))
巻:
18
号:
1
ページ:
3
発行年:
2017年
JST資料番号:
U7366A
ISSN:
1471-2156
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)