Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease.
作者:
Christoph,Preuss [1]
;
Melanie,Capredon [1]
;
Florian,Wünnemann [1]
;
Philippe,Chetaille [2]
;
Andrea,Prince [3]
;
Beatrice,Godard [1]
;
Severine,Leclerc [4]
;
Nara,Sobreira [1]
;
Hua,Ling [5]
;
Philip,Awadalla [5]
;
Maryse,Thibeault [6]
;
Paul,Khairy [1]
;
MIBAVA Leducq consortium [7]
;
Mark E,Samuels [8]
;
Gregor,Andelfinger [9]
作者单位:
Cardiovascular Genetics, Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montreal, Québec, Canada.
[1]
Faculty of Biology, University of Muenster, Muenster, Germany.
[2]
Department of Pediatrics, Centre Mère Enfants Soleil, Centre Hospitalier de l'Université (CHU) de Québec, Quebec City, Québec, Canada.
[3]
Omics-Ethics Research Group, Research Institute of Public Health, Université de Montréal, Montréal Québec, Canada.
[4]
McKusick Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
[5]
Ontario Institute for Cancer Research, Toronto, Ontario, Canada.
[6]
Montreal Heart Institute, Université de Montréal, Montréal, Québec, Canada.
[7]
Centre de Recherche CHU Sainte Justine, Université de Montreal, Montréal, Québec, Canada.
[8]
Department of Medicine, Université de Montreal, Montréal, Québec, Canada.
[9]
期刊:
《PLoS genetics》
2016年12卷10期e1006335页
DOI:
10.1371/journal.pgen.1006335
PMID:
27760138
发布时间:
2018-11-13
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