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Rare copy number variants and congenital heart defects in t..:
The International Chromosome 22q11.2 Consortium
;
Mlynarski, Elisabeth E.
;
Xie, Michael
...
Human Genetics. 135 (2016) 3 - p. 273-285 , 2016
Link:
https://doi.org/10.1007/s00439-015-1623-9
RT Journal T1
Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome
UL https://suche.suub.uni-bremen.de/peid=cr-10.1007_s00439-015-1623-9&Exemplar=1&LAN=DE A1 The International Chromosome 22q11.2 Consortium A1 Mlynarski, Elisabeth E. A1 Xie, Michael A1 Taylor, Deanne A1 Sheridan, Molly B. A1 Guo, Tingwei A1 Racedo, Silvia E. A1 McDonald-McGinn, Donna M. A1 Chow, Eva W. C. A1 Vorstman, Jacob A1 Swillen, Ann A1 Devriendt, Koen A1 Breckpot, Jeroen A1 Digilio, Maria Cristina A1 Marino, Bruno A1 Dallapiccola, Bruno A1 Philip, Nicole A1 Simon, Tony J. A1 Roberts, Amy E. A1 Piotrowicz, Małgorzata A1 Bearden, Carrie E. A1 Eliez, Stephan A1 Gothelf, Doron A1 Coleman, Karlene A1 Kates, Wendy R. A1 Devoto, Marcella A1 Zackai, Elaine A1 Heine- Suñer, Damian A1 Goldmuntz, Elizabeth A1 Bassett, Anne S. PB Springer Science and Business Media LLC YR 2016 SN 0340-6717 SN 1432-1203 JF Human Genetics VO 135 IS 3 SP 273 OP 285 LK http://dx.doi.org/https://doi.org/10.1007/s00439-015-1623-9 DO https://doi.org/10.1007/s00439-015-1623-9 SF ELIB - SuUB Bremen
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