Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome
ContributorsMlynarski, Elisabeth E.; Xie, Michael; Taylor, Deanne; Sheridan, Molly B.; Guo, Tingwei; Racedo, Silvia E.; McDonald-McGinn, Donna M.; Chow, Eva W. C.; Vorstman, Jacob; Swillen, Ann; Devriendt, Koen; Breckpot, Jeroen; Digilio, Maria Cristina; Marino, Bruno; Dallapiccola, Bruno; Philip, Nicole; Simon, Tony J.; Roberts, Amy E.; Piotrowicz, Małgorzata; Bearden, Carrie E.; Eliez, Stéphan; Gothelf, Doron; Coleman, Karlene; Kates, Wendy R.; Devoto, Marcella; Zackai, Elaine; Heine- Suñer, Damian; Goldmuntz, Elizabeth; Bassett, Anne S.; Morrow, Bernice E.; Emanuel, Beverly S.; International Chromosome 22q11.2 Consortium
Published inHuman genetics, vol. 135, no. 3, p. 273-285
Publication date2016
Affiliation entities
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
Main files (1)
Article (Published version)
Identifiers
- PID : unige:82909
- DOI : 10.1007/s00439-015-1623-9
Additional URL for this publicationhttp://link.springer.com/10.1007/s00439-015-1623-9
Journal ISSN0340-6717
