Article info

Download PDFPDF

Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13
Free
  1. Correspondence to:
 Dr F R Goodman, Room 213, Molecular Medicine Unit, Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK;
 fgoodman{at}hgmp.mrc.ac.uk
View Full Text

Citation

Debeer P, Bacchelli C, Scambler PJ, et al
Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13

Publication history

  • First published November 1, 2002.
Online issue publication 
November 01, 2002

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.