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 Journal Articles Unrefereed Letters or Notes uri icon

Overview

Published in

  • European Journal of Medical Genetics

Time

Date/time value

  • 2017

Identity

Digital Object Identifier (DOI)

  • 10.1016/j.ejmg.2017.10.001

Additional Document Info

Parent Title

  • EUROPEAN JOURNAL OF MEDICAL GENETICS
  • European Journal of Medical Genetics

Volume

  • 61

Issue

  • 1

Publisher

  • Elsevier Masson