Cite
HARVARD Citation
Voigt, R. et al. (2002). Chromosome 10p13-14 and 22q11 deletion screening in 100 patients with isolated and syndromic conotruncal heart defects. Journal of medical genetics. 39 (4), p. e16. [Online].
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Voigt, R. et al. (2002). Chromosome 10p13-14 and 22q11 deletion screening in 100 patients with isolated and syndromic conotruncal heart defects. Journal of medical genetics. 39 (4), p. e16. [Online].