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Consensus recommendations on communication, language and speech in Phelan-McDermid syndrome

  • Published:2023-05 Issue:5 Volume:66 Page:104745
  • ISSN:1769-7212
  • Container-title:European Journal of Medical Genetics
  • language:en
  • Short-container-title:European Journal of Medical Genetics

Author:

Burdeus-Olavarrieta MonicaORCID,Nevado Julián,van Weering-Scholten Sabrina,Parker Susanne,Swillen Ann

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference42 articles.

1. Diagnostic and statistical manual of mental disorders,2022

2. Speech and language phenotype in Phelan-McDermid (22q13.3) syndrome;Brignell;Eur. J. Hum. Genet.,2020

3. AGREE II: advancing guideline development, reporting and evaluation in health care;Brouwers;CMAJ (Can. Med. Assoc. J.),2010

4. Characterisation of the clinical phenotype in Phelan-McDermid syndrome;Burdeus-Olavarrieta;J. Neurodev. Disord.,2021

5. Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations;De Rubeis;Mol. Autism.,2018

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