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1 Ergebnisse
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Complete Sequence of the 22q11.2 Allele in 1,053 Subjects w..:
Zhao, Yingjie
;
Diacou, Alexander
;
Johnston, H. Richard
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7077921/. , 2020
Link:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7077921/
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-ftpubmed:oai:pubmedcentral.nih.gov:7077921&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 Bearden, Carrie E A1 Vingerhoets, Claudia A1 van Amelsvoort, Therese A1 Eliez, Stephan A1 Schneider, Maude A1 Vorstman, Jacob A.S A1 Gothelf, Doron A1 Zackai, Elaine A1 Agopian, A.J 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 Elsevier YR 2020 K1 Article JF http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7077921/ LK http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7077921/ DO http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7077921/ SF ELIB - SuUB Bremen
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