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.

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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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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0010-8C5C-E Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0010-8C5D-C

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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: Date issued: 2002-02

Publication Status: Issued

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Identifiers: eDoc: 24364

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Title: Journal of Medical Genetics

Source Genre: Journal

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Pages: - Volume / Issue: 39 (4) Sequence Number: - Start / End Page: e16 - e16 Identifier: -