A case of multiple congenital anomalies in association with Rett syndrome confirmed by MECP2 mutation screening Journal Articles uri icon

Overview

Published in

  • Clinical Dysmorphology

Time

Date/time value

  • 2001

Identity

Digital Object Identifier (DOI)

  • 10.1097/00019605-200107000-00006

Additional Document Info

Parent Title

  • CLINICAL DYSMORPHOLOGY

Volume

  • 10

Issue

  • 3

Publisher

  • Lippincott Williams & Wilkins