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Your search keyword '"Gérard, Bénédicte"' showing total 7 results

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7 results on '"Gérard, Bénédicte"'

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1. Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study

2. Correction: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study

3. The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant

4. Primrose syndrome: a phenotypic comparison of patients with a ZBTB20 missense variant versus a 3q13.31 microdeletion including ZBTB20

5. Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome

6. 20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition

7. 20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition.

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