7 results on '"Gérard, Bénédicte"'
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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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