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

MPS-Authors

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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Citation

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