Extending the clinical and genetic spectrum of ARID2 related intellectual disability. A case series of 7 patients - ScienceDirect
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Descrição
Multiplex gene and phenotype network to characterize shared
Pan-cancer proteogenomics connects oncogenic drivers to functional
Driver mutations in ADGRL3 are involved in the evolution of
Extending the clinical and genetic spectrum of ARID2 related
Integrative Functional Genomic Analyses Implicate Specific
Extending the clinical and genetic spectrum of ARID2 related
Advancing the understanding of autism disease mechanisms through
Neurobiology of ARID1B haploinsufficiency related to
Description of neurodevelopmental phenotypes associated with 10
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