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  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.

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 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              

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Free keywords: conotruncal heart defects; 22q11 deletion; 10p13-14 deletion
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Language(s): eng - English
 Dates: 2002-02
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: -
 Identifiers: eDoc: 24364
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Title: Journal of Medical Genetics
Source Genre: Journal
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Publ. Info: -
Pages: - Volume / Issue: 39 (4) Sequence Number: - Start / End Page: e16 - e16 Identifier: -