Valérie Malan
0000-0002-3450-4958
3 papers found
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Prenatal findings in 1p36 deletion syndrome: New cases and a literature review
Chromosomal microarray analysis in fetuses with an isolated congenital heart defect: A retrospective, nationwide, multicenter study in France
Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter study
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