English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  Chromosome 10p13-14 and 22q11 deletion screening in 100 patients with isolated and syndromic conotruncal heart defects

Voigt, R., Maier-Weidmann, M., Lange, P. E., & Haaf, T. (2002). Chromosome 10p13-14 and 22q11 deletion screening in 100 patients with isolated and syndromic conotruncal heart defects. Journal of Medical Genetics, 39(4), e16-e16.

Item is

Files

show Files

Locators

show

Creators

show
hide
 Creators:
Voigt, R.1, Author
Maier-Weidmann, M., Author
Lange, P. E., Author
Haaf, T.2, Author              
Affiliations:
1Max Planck Society, ou_persistent13              
2Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433549              

Content

show
hide
Free keywords: conotruncal heart defects; 22q11 deletion; 10p13-14 deletion
 Abstract: -

Details

show
hide
Language(s): eng - English
 Dates: 2002-02
 Publication Status: Published in print
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: eDoc: 24364
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Journal of Medical Genetics
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 39 (4) Sequence Number: - Start / End Page: e16 - e16 Identifier: -