TY  - GEN
AU  - Zeesman,Susan
AU  - Nowaczyk,Małgorzata J M
AU  - Teshima,Ikuko
AU  - Roberts,Wendy
AU  - Cardy,Janis Oram
AU  - Brian,Jessica
AU  - Senman,Lili
AU  - Feuk,Lars
AU  - Osborne,Lucy R
AU  - Scherer,Stephen W
TI  - Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2
SN  - 1552-4825
PY  - 2006///0530
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Apraxias
KW  - pathology
KW  - Child, Preschool
KW  - Chromosome Banding
KW  - Chromosome Deletion
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 7
KW  - Female
KW  - Forkhead Transcription Factors
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Karyotyping
KW  - Language Disorders
KW  - Microsatellite Repeats
KW  - Speech Disorders
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.a.31110
ER  -