6 results on '"Bedoyan, Jirair K."'
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2. Novel SMC1A frameshift mutations in children with developmental delay and epilepsy
3. The impact of serotonin transporter (5-HTTLPR) genotype on the development of resting-state functional connectivity in children and adolescents: A preliminary report
4. A novel GK Ala469Val variant resulting in glycerol kinase deficiency with concurrent hepatoblastoma: A case report
5. Novel presentations associated with a PDHA1 variant – Alternating hemiplegia in Hemizygote proband and Guillain Barre Syndrome in Heterozygote mother
6. First case of deletion of the faciogenital dysplasia 1 ( FGD1) gene in a patient with Aarskog–Scott syndrome
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