Letter regarding the article "Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals (Bijlsma et al., 2009)" and the diagnosis of coexisting Mowat-Wilson syndrome in a patient with 16p11.2 deletion

Author(s):
Amor, D.J.; Bijlsma, E.K.
Published
2018
Publication type
Article / Letter to editor
16p11.2 deletionMowat-Wilson syndromeZEB2
Date issued
2018-01-31
Language
English
Is part of
European Journal of Medical Genetics (2018), Vol. 61, no. 1, p. 48-49
hdl
1887/119459
doi
10.1016/j.ejmg.2017.10.001