A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2 Journal Articles Refereed uri icon

Overview

Published in

  • European Journal of Human Genetics

Time

Date/time value

  • 2016

Identity

Digital Object Identifier (DOI)

  • 10.1038/ejhg.2015.149

Additional Document Info

Parent Title

  • EUROPEAN JOURNAL OF HUMAN GENETICS

Volume

  • 24

Issue

  • 2

Publisher

  • Nature Publishing Group