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1 Ergebnisse
1
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects w..:
Zhao, Yingjie
;
Diacou, Alexander
;
Johnston, H Richard
...
qt38b9f8cx. , 2020
Link:
https://escholarship.org/uc/item/38b9f8cx
RT Journal T1
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt38b9f8cx&Exemplar=1&LAN=DE A1 Zhao, Yingjie A1 Diacou, Alexander A1 Johnston, H Richard A1 Musfee, Fadi I A1 McDonald-McGinn, Donna M A1 McGinn, Daniel A1 Crowley, T Blaine A1 Repetto, Gabriela M A1 Swillen, Ann A1 Breckpot, Jeroen A1 Vermeesch, Joris R A1 Kates, Wendy R A1 Digilio, M Cristina A1 Unolt, Marta A1 Marino, Bruno A1 Pontillo, Maria A1 Armando, Marco A1 Di Fabio, Fabio A1 Vicari, Stefano A1 van den Bree, Marianne A1 Moss, Hayley A1 Owen, Michael J A1 Murphy, Kieran C A1 Murphy, Clodagh M A1 Murphy, Declan A1 Schoch, Kelly A1 Shashi, Vandana A1 Tassone, Flora A1 Simon, Tony J A1 Shprintzen, Robert J A1 Campbell, Linda A1 Philip, Nicole A1 Heine-Suñer, Damian A1 García-Miñaúr, Sixto A1 Fernández, Luis A1 Consortium, International 22q11 2 Brain and Behavior A1 Antonarakis, Stylianos E A1 Biondi, Massimo A1 Boot, Erik A1 Breetvelt, Elemi A1 Busa, Tiffany A1 Butcher, Nancy A1 Buzzanca, Antonino A1 Carmel, Miri A1 Cleynen, Isabelle A1 Cutler, David A1 Dallapiccola, Bruno A1 de la Fuente Sanches, María Angeles A1 Epstein, Michael P A1 Evers, Rens A1 Fernandez, Luis A1 Fritsch, Rosemarie A1 Algas, Fernando García A1 Guo, Tingwei A1 Gur, Raquel A1 Hestand, Matthew S A1 Heung, Tracy A1 Hooper, Stephen A1 Jin, Andrea A1 Kushan-Wells, Leila A1 Laorden-Nieto, Alejandra Teresa A1 Lattanzi, Guido A1 Marshall, Christian A1 McCabe, Kathryn A1 Michaelovsky, Elena A1 Ornstein, Claudia A1 Silversides, Candice A1 Tran, Oanh A1 van Duin, Esther DA A1 Vergaelen, Elfi A1 Warren, Steve T A1 Weinberger, Ronnie A1 Weizman, Abraham A1 Zhang, Zhengdong A1 Zwick, Michael A1 Bearden, Carrie E A1 Vingerhoets, Claudia A1 van Amelsvoort, Therese A1 Eliez, Stephan A1 Schneider, Maude A1 Vorstman, Jacob AS A1 Gothelf, Doron A1 Zackai, Elaine A1 Agopian, AJ A1 Gur, Raquel E A1 Bassett, Anne S A1 Emanuel, Beverly S A1 Goldmuntz, Elizabeth A1 Mitchell, Laura E A1 Wang, Tao A1 Morrow, Bernice E PB eScholarship, University of California YR 2020 K1 Biological Sciences K1 Biomedical and Clinical Sciences K1 Genetics K1 Epidemiology K1 Health Sciences K1 Clinical Research K1 Human Genome K1 Heart Disease K1 Cardiovascular K1 Pediatric K1 Aetiology K1 2.1 Biological and endogenous factors K1 Case-Control Studies K1 Chromosome Deletion K1 Chromosomes K1 Human K1 Pair 22 K1 Cohort Studies K1 Female K1 Genome-Wide Association Study K1 Heart Defects K1 Congenital K1 Humans K1 Linkage Disequilibrium K1 Male K1 Phenotype K1 Polymorphism K1 Single Nucleotide K1 Proto-Oncogene Mas K1 Segmental Duplications K1 Genomic K1 International 22q11.2 Brain and Behavior Consortium K1 CRKL K1 DiGeorge syndrome K1 TBX1 K1 chromosome 22q11.2 deletion syndrome K1 complex trait K1 congenital heart disease K1 conotruncal heart defects K1 copy number variation K1 genetic association K1 genetic modifier K1 haploinsufficiency K1 Medical and Health Sciences K1 Genetics & Heredity JF qt38b9f8cx LK http://dx.doi.org/https://escholarship.org/uc/item/38b9f8cx DO https://escholarship.org/uc/item/38b9f8cx SF ELIB - SuUB Bremen
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