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
UNIGE affiliation entities
UNIGE research groups
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
