Items where Author is "Song, Y."

Article

(2024) Molecular and phenotypical findings of a novel de novo SYNGAP1 gene variant in an 11-year-old Iranian boy with intellectual disability. Laboratory medicine. pp. 204-208. ISSN 1943-7730 (Electronic) 0007-5027 (Linking)

(2024) A novel de novo frameshift variant in the CHD2 gene related to intellectual and developmental disability, seizures and speech problems. Molecular Genetics & Genomic Medicine. e2305. ISSN 2324-9269 (Electronic) 2324-9269 (Linking)

(2023) Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literature. Bmc Medical Genomics. p. 20.