Coffin–Siris syndrome and related disorders involving components of the BAF (mSWI/SNF) complex: Historical review and recent advances using next generation sequencing
Clinical features, diagnostic criteria, and management of Coffin–Siris syndrome
Numerous BAF complex genes are mutated in Coffin–Siris syndrome
Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1 , SMARCA4 , SMARCE1 , and ARID1A
The ARID1B phenotype: What we have learned so far
Females with de novo aberrations in PHF6 : Clinical overlap of Borjeson–Forssman–Lehmann with Coffin–Siris syndrome
Phenotype and genotype in Nicolaides–Baraitser syndrome
The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism
DOORS syndrome: Phenotype, genotype and comparison with Coffin-Siris syndrome
The role of BAF (mSWI/SNF) complexes in mammalian neural development
SWI/SNF chromatin remodeling complexes and cancer