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Scientific article
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Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome

Published inHuman genetics, vol. 135, no. 3, p. 273-285
Publication date2016
Citation (ISO format)
MLYNARSKI, Elisabeth E. et al. Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome. In: Human genetics, 2016, vol. 135, n° 3, p. 273–285. doi: 10.1007/s00439-015-1623-9
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ISSN of the journal0340-6717
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Creation04/15/2016 9:11:00 AM
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