Molka Kammoun
2PUBLICATIONS
8CO-AUTHORS
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Publications (2)
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|Sep 03, 2019
Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition.Marta Unolt, Molka Kammoun, Beata Nowakowska
|Jul 03, 2018
Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next-generation sequencing.Molka Kammoun, Erika Souche, Paul Brady
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