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

Affiliations

¹ Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia; Department of Paediatrics, The University of Melbourne, Victoria, Australia. Electronic address: david.amor@mcri.edu.au.
² Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.

Comment

David J Amor et al. Eur J Med Genet. 2018 Jan.

. 2018 Jan;61(1):48-49.

doi: 10.1016/j.ejmg.2017.10.001. Epub 2017 Oct 9.

¹ Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia; Department of Paediatrics, The University of Melbourne, Victoria, Australia. Electronic address: david.amor@mcri.edu.au.
² Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.

No abstract available

Keywords: 16p11.2 deletion; Mowat-Wilson syndrome; ZEB2.

Comment on

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.
Bijlsma EK, Gijsbers AC, Schuurs-Hoeijmakers JH, van Haeringen A, Fransen van de Putte DE, Anderlid BM, Lundin J, Lapunzina P, Pérez Jurado LA, Delle Chiaie B, Loeys B, Menten B, Oostra A, Verhelst H, Amor DJ, Bruno DL, van Essen AJ, Hordijk R, Sikkema-Raddatz B, Verbruggen KT, Jongmans MC, Pfundt R, Reeser HM, Breuning MH, Ruivenkamp CA. Bijlsma EK, et al. Eur J Med Genet. 2009 Mar-Jun;52(2-3):77-87. doi: 10.1016/j.ejmg.2009.03.006. Epub 2009 Mar 21. Eur J Med Genet. 2009. PMID: 19306953