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Filters: Author is Pichon, Olivier [Clear All Filters]
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2016. Search for Rare Copy-Number Variants in Congenital Heart Defects Identifies Novel Candidate Genes and a Potential Role for FOXC1 in Patients With Coarctation of the Aorta. Circulation: Cardiovascular Genetics. 9:86–94.
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2015. Phenotype-genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature.. Am J Med Genet A. 167A(1):111-22.
