Extending the clinical and genetic spectrum of ARID2 related intellectual disability. A case series of 7 patients - ScienceDirect
Por um escritor misterioso
Descrição
Vitiligo and melanocytic nevi: New findings in Coffin-Siris
Genetic heterogeneity in autism: From single gene to a pathway
Retrospective analysis of a clinical exome sequencing cohort
PDF) Mutations in ARID2 are associated with intellectual disabilities
Multiplex gene and phenotype network to characterize shared
Chromatin dynamics in human brain development and disease: Trends
Pan-cancer proteogenomics connects oncogenic drivers to functional
PDF] Genetic Testing for Developmental Disabilities, Intellectual
Extending the clinical and genetic spectrum of ARID2 related
PDF) Generation of an iPSC line (CRICKi001-A) from an individual
