Article Text

Download PDFPDF

Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus.
  1. M Sharland,
  2. R Taylor,
  3. M A Patton,
  4. S Jeffery
  1. South West Thames Regional Genetic Service, St George's Hospital Medical School, London.

    Abstract

    Eleven families with Noonan syndrome in either two or three generations have been identified. Following the reports of subjects with features of both Noonan syndrome and neurofibromatosis type 1, these pedigrees have been studied using a number of probes at the neurofibromatosis type 1 locus (17q11). A significantly negative lod score was obtained with the intragenic probe NF1-C2, suggesting that the genes for Noonan syndrome and neurofibromatosis type 1 are not contiguous.

    Statistics from Altmetric.com

    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.