Leila Ghesh (Leïla Ghesh)

Years Active: 2019-2021
Publications (10 Years): 3

This page only lists publications with an associated author ORCID identifier.

Publications

Leila Ghesh, Thomas Besnard, Mathilde Nizon, Eva Trochu, Gaëlle Landeau-Trottier, Flora Breheret, Christel Thauvin-Robinet, Ange-Line Bruel, Paul Kuentz, Christine Coubes, Laurence Cuisset, Cyril Mignot, Boris Keren, Stéphane Bézieau, Benjamin Cogné
Loss-of-function variants in ARHGEF9 are associated with an X-linked intellectual disability dominant disorder. Human mutation 42 (5) (2021)
Leila Ghesh, Marie Denis Musquer, Louise Devisme, Morgane Stichelbout, Lucile Boutaud, Nadia Elkhartoufi, Pascal Vaast, Odile Boute, Anne-Sophie Riteau, Claudine Le Vaillant, Norbert Winer, Madeleine Joubert, Stéphane Bezieau, Sophie Thomas, Tania Attie-Bitach, Claire Beneteau
The first two non-Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome. Clinical genetics 100 (4) (2021)
Leila Ghesh, Marie Vincent, Anne-Sophie Delemazure, Julie Boyer, Pierre Corre, Fabienne Perez, David Geneviève, Jean-Louis Laplanche, Corinne Collet, Bertrand Isidor
Autosomal recessive Treacher Collins syndrome due to POLR1C mutations: Report of a new family and review of the literature. American journal of medical genetics. Part A 179 (7) (2019)

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