Thierry Bienvenu
0000-0002-5953-2728
3 papers found
Refreshing results…
Further delineation of the female phenotype with KDM5C disease causing variants: 19 new individuals and review of the literature
Wiedemann-Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French cases
Autism spectrum disorder recurrence, resulting of germline mosaicism for a CHD2 gene missense variant: Letter to the Editor
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