Article info
PDFElectronic letters
Chromosome 10p13-14 and 22q11 deletion screening in 100 patients with isolated and syndromic conotruncal heart defects
- Correspondence to: Dr T Haaf, Institute of Human Genetics, Mainz University School of Medicine, Langenbeckstrasse 1, Bldg 601, 55131 Mainz, Germany; Haaf{at}humgen.klinik.uni-mainz.de
Citation
Chromosome 10p13-14 and 22q11 deletion screening in 100 patients with isolated and syndromic conotruncal heart defects
Publication history
- First published April 1, 2002.
Online issue publication
April 27, 2016
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.
Copyright information
Copyright 2002 Journal of Medical Genetics