1p13.2 deletion displays clinical features overlapping Noonan syndrome, likely related to NRAS gene haploinsufficiency Journal Articles Refereed uri icon

Overview

Authors

  • Authorship

    • LINHARES ND
    • THURESSON A-C
    • ANNEREN G
    • PENA SDJ
    • MENEZES FREIRE MC
    • DO CARMO LISBOA CARDENAS RGC
    • PENA HB
    • LACHLAN K
    • DALLAPICCOLA B
    • BACINO C
    • DELOBEL B
    • A/PROF Paul James

Published in

  • Genetics and Molecular Biology

Time

Date/time value

  • 2016

Identity

Digital Object Identifier (DOI)

  • 10.1590/1678-4685-GMB-2016-0049

Additional Document Info

Parent Title

  • GENETICS AND MOLECULAR BIOLOGY

Volume

  • 39

Issue

  • 3

Publisher

  • Sociedade Brasileira de Genetica