关键词: 3p13 FOXP1 chromosomal microdeletion intellectual disability speech-language pathology
Mesh : Animals Autistic Disorder / genetics physiopathology Child Developmental Disabilities / genetics physiopathology Forkhead Transcription Factors / genetics Haploinsufficiency / genetics Humans Intellectual Disability / genetics physiopathology Male Mice Mutation Phenotype Repressor Proteins / genetics Sequence Deletion / genetics
来 源:
DOI:10.1002/ajmg.a.36174
PDF(Sci-hub)