Persistent URL of this record https://hdl.handle.net/1887/119459
In Collections
This item can be found in the following collections:
![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](https://scholarlypublications.universiteitleiden.nl/sites/all/themes/scholarly/img/closed_access.png)
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
- All authors
- Amor, D.J.; Bijlsma, E.K.
- Date
- 2018-01-31
- Volume
- 61
- Issue
- 1
- Pages
- 48 - 49