@article{article, title  = {{Speech, language and communication phenotyping in rare genetic syndromes: Commentary on Speech and language deficits are central to SETBP1 haploinsufficiency disorder}},

 publisher = {{Springer Science and Business Media LLC}},

 url = {{https://eprints.whiterose.ac.uk/178419/ }},

 year = {{2021}},

 month = {{8}},

 author = {{Freeth M and Al-Jawahiri R and Smith H and Stokes L}},

 doi = {{10.1038/s41431-021-00942-6}},

 volume = {{29}},

 journal = {{European Journal of Human Genetics}},

 issue = {{8}},

 pages = {{1166-1167}},

 note = {{Accessed on 2024/09/19}}}