Speech, language and communication phenotyping in rare genetic syndromes: Commentary on Speech and language deficits are central to SETBP1 haploinsufficiency disorder
Crossref DOI link: https://doi.org/10.1038/s41431-021-00942-6
Published Online: 2021-08-20
Published Print: 2021-08
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Freeth, Megan
Al-Jawahiri, Reem
Smith, Harriet
Stokes, Louis
Text and Data Mining valid from 2021-08-01
Version of Record valid from 2021-08-01
Article History
First Online: 20 August 2021
Competing interests
: The authors declare no competing interests.