You are here

  • Home
  • Archive
  • Volume 35, Issue 8
  • Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23.

Article info

Article menu

Download PDFPDF

Research Article
Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23.
Free

Authors

    Citation

    Mowat DR, Croaker GD, Cass DT, et al
    Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23.
    Journal of Medical Genetics 1998;35:617-623.

    Publication history

    • First published August 1, 1998.
    Online issue publication 
    August 01, 1998

    Request permissions

    If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.