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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Edwige Kasper

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Clinical Genetics|January 17, 2021

Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic ConsortiumFlavie Boulouard, Edwige Kasper, Marie-Pierre Buisine, et al.

Journal of Medical Genetics|October 27, 2017

Contribution of de novo and mosaic <i>TP53</i> mutations to Li-Fraumeni syndromeMariette Renaux-Petel, Françoise Charbonnier, Jean-Christophe Théry, et al.

European Journal of Human Genetics : EJHG|June 28, 2020

Detection of copy-number variations from NGS data using read depth information: a diagnostic performance evaluationOlivier Quenez, Kevin Cassinari, Sophie Coutant, et al.

International Journal of Cancer|June 12, 2025

Deciphering dual clinical entities associated with TP53 pathogenic variants: Insights from 53,085 HBOC panel analyses in French laboratoriesEdwige Kasper, Flavie Boulouard, Noémie Basset, et al.

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Search research articles

Showing results (11-20 of 14) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 14 results.

Clinical Genetics|January 17, 2021

Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic ConsortiumFlavie Boulouard, Edwige Kasper, Marie-Pierre Buisine, et al.

Journal of Medical Genetics|October 27, 2017

Contribution of de novo and mosaic <i>TP53</i> mutations to Li-Fraumeni syndromeMariette Renaux-Petel, Françoise Charbonnier, Jean-Christophe Théry, et al.

European Journal of Human Genetics : EJHG|June 28, 2020

Detection of copy-number variations from NGS data using read depth information: a diagnostic performance evaluationOlivier Quenez, Kevin Cassinari, Sophie Coutant, et al.

International Journal of Cancer|June 12, 2025

Deciphering dual clinical entities associated with TP53 pathogenic variants: Insights from 53,085 HBOC panel analyses in French laboratoriesEdwige Kasper, Flavie Boulouard, Noémie Basset, et al.

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