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
Zdroj: PLoS ONE. 2010, Vol. 5 Issue 5, p1-7. 7p. 2 Charts, 2 Graphs.
Databáze: Academic Search Ultimate