14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype Journal Articles Refereed uri icon

Overview

Authors

  • Authorship

    • ELLAWAY CJ
    • FAGAN K
    • PROF John Christodoulou
    • HO G
    • BETTELLA E
    • KNAPMAN A
    • COLLINS F
    • HACKETT A
    • MCKENZIE F
    • DARMANIAN A
    • PETERS GB

Published in

  • European Journal of Human Genetics

Time

Date/time value

  • 2013

Identity

Digital Object Identifier (DOI)

  • 10.1038/ejhg.2012.208

Additional Document Info

Parent Title

  • EUROPEAN JOURNAL OF HUMAN GENETICS

Volume

  • 21

Issue

  • 5

Publisher

  • Nature Publishing Group