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