Résultats de la recherche

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(1 - 3 of 3)
Long term follow up of two independent patients with Schinzel-Giedion carrying SETBP1 mutations
20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition
Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing

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