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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.

Pubmed ID: 
29024826
Year: 
2018
Month: 
01
Volume: 
61
Issue: 
1
Citation: 
Amor DJ, Bijlsma EK. 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. European journal of medical genetics 61 (1) : 48 - 49(2018) PubMed
Pubmed Link: 
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=29024826&dopt=Abstract