Laura Mary
5PUBLICATIONS
4CO-AUTHORS
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Publications (5)
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|Nov 05, 2024
Identification and Characterization of Novel FSHR Copy Number Variations Causing Premature Ovarian Insufficiency.Anna Lokchine, Anne Bergougnoux, Nadège Servant
|Feb 25, 2023
Functional Assessment of a New PBX1 Variant in a 46,XY Fetus with Severe Syndromic Difference of Sexual Development through CRISPR-Cas9 Gene Editing.Laura Mary, Delphine Leclerc, Audrey Labalme
|Apr 22, 2022
The TALE never ends: A comprehensive overview of the role of PBX1, a TALE transcription factor, in human developmental defects.Laura Mary, Delphine Leclerc, David Gilot
|Mar 23, 2021
Pathogenic variants in KCNQ2 cause intellectual deficiency without epilepsy: Broadening the phenotypic spectrum of a potassium channelopathy.Laura Mary, Elsa Nourisson, Claire Feger
|Mar 30, 2019
Genetic kinship and admixture in Iron Age Scytho-Siberians.Laura Mary, Vincent Zvénigorosky, Alexey Kovalev
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