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

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Voigt, R.
Max Planck Society;

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Haaf, T.
Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;

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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.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0010-8C5C-E

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