TY  - JOUR

T1  - Speech, language and communication phenotyping in rare genetic syndromes: Commentary on Speech and language deficits are central to SETBP1 haploinsufficiency disorder

JO  - European Journal of Human Genetics

UR  - https://eprints.whiterose.ac.uk/178419/

PY  - 2021/08/01

AU  - Freeth M

AU  - Al-Jawahiri R

AU  - Smith H

AU  - Stokes L

ED  - 

DO  - DOI: 10.1038/s41431-021-00942-6

PB  - Springer Science and Business Media LLC

VL  - 29

IS  - 8

SP  - 1166

EP  - 1167

Y2  - 2024/12/22

ER  -