Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16
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2005 ◽
Vol 26
(20)
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pp. 2179-2184
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1971 ◽
Vol 81
(5)
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pp. 720-722
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2008 ◽
Vol 72
(3)
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pp. 416-423
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2020 ◽
Vol 5
(02)
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