Alejandro Sifrim
0000-0001-8247-4020
3 papers found
Refreshing results…
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease
Clinical and molecular consequences of disease-associated de novo mutations in SATB2
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing
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