Common Variation in ISL1 Confers Genetic Susceptibility for Human Congenital Heart Disease.
Autor: | Stevens, Kristen N.1, Hakonarson, Hakon2, Kim, Cecilia E.2, Doevendans, Pieter A.3, Koeleman, Bobby P. C.4, Mital, Seema5, Raue, Jennifer2, Glessner, Joseph T.2, Coles, John G.5, Moreno, Victor6, Granger, Anne2, Gruber, Stephen B.1,7,8 sgruber@umich.edu, Gruber, Peter J.2,9,10 pgruber@mail.med.upenn.edu |
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Zdroj: | PLoS ONE. 2010, Vol. 5 Issue 5, p1-7. 7p. 2 Charts, 2 Graphs. |
Databáze: | Academic Search Ultimate |
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