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Common variation in ISL1 confers genetic susceptibility for human congenital heart disease
Stevens, K.N.; Hakonarson, H.; Kim, C.E.; Doevendans, P.A.; Koeleman, B.P.; Mital, S.; Raue, J.; Glessner, J.T.; Coles, J.G.; Moreno Aguado, Víctor; Granger, A.; Gruber, S.B.; Gruber, PJ.
Universitat de Barcelona
Malalties coronàries
Estudi de casos
Malformacions del cor
Genètica
Coronary diseases
Case studies
Heart abnormalities
Genetics
cc-by (c) Stevens, K.N. et al., 2010
http://creativecommons.org/licenses/by/3.0/es
Article
info:eu-repo/semantics/publishedVersion
Public Library of Science (PLoS)
         

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