TY  - GEN
AU  - Zarate,Yuri A
AU  - Perry,Hazel
AU  - Ben-Omran,Tawfeg
AU  - Sellars,Elizabeth A
AU  - Stein,Quinn
AU  - Almureikhi,Mariam
AU  - Simmons,Kirk
AU  - Klein,Ophir
AU  - Fish,Jennifer
AU  - Feingold,Murray
AU  - Douglas,Jessica
AU  - Kruer,Michael C
AU  - Si,Yue
AU  - Mao,Rong
AU  - McKnight,Dianalee
AU  - Gibellini,Federica
AU  - Retterer,Kyle
AU  - Slavotinek,Anne
TI  - Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing
SN  - 1552-4833
PY  - 2016///0108
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Chromosomes, Human, Pair 2
KW  - genetics
KW  - Cleft Palate
KW  - Codon, Nonsense
KW  - Craniofacial Abnormalities
KW  - Exome
KW  - Female
KW  - Frameshift Mutation
KW  - High-Throughput Nucleotide Sequencing
KW  - Humans
KW  - Intellectual Disability
KW  - Language Development Disorders
KW  - Male
KW  - Matrix Attachment Region Binding Proteins
KW  - Transcription Factors
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1002/ajmg.a.36849
ER  -