Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study Journal Articles Refereed uri icon

Overview

Published in

  • Genetics in Medicine

Time

Date/time value

  • 2013

Identity

Digital Object Identifier (DOI)

  • 10.1038/gim.2012.134

Additional Document Info

Parent Title

  • GENETICS IN MEDICINE

Volume

  • 15

Issue

  • 4

Publisher

  • Lippincott Williams & Wilkins