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Letter regarding the article "Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals ()" and the diagnosis of coexisting Mowat-Wilson syndrome in a patient with 16p11.2 deletion.

Authors
  • Amor, David J1
  • Bijlsma, Emilia K2
  • 1 Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia; Department of Paediatrics, The University of Melbourne, Victoria, Australia. Electronic address: [email protected] , (Australia)
  • 2 Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands. , (Netherlands)
Type
Published Article
Journal
European journal of medical genetics
Publication Date
Oct 09, 2017
Identifiers
DOI: 10.1016/j.ejmg.2017.10.001
PMID: 29024826
Source
Medline
Keywords
License
Unknown
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