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Rare variants in CAPN2 increase risk for isolated hypoplast..:
National Birth Defects Prevention Study
;
University of Washington Center for Mendelian Genomics
;
Blue, Elizabeth E
...
10.1016/j.xhgg.2023.100232. , 2023
Link:
http://hdl.handle.net/10138/566230
RT Journal T1
Rare variants in CAPN2 increase risk for isolated hypoplastic left heart syndrome
UL https://suche.suub.uni-bremen.de/peid=base-ftunivhelsihelda:oai:helda.helsinki.fi:10138_566230&Exemplar=1&LAN=DE A1 National Birth Defects Prevention Study A1 University of Washington Center for Mendelian Genomics A1 Blue, Elizabeth E A1 White, Janson J A1 Dush, Michael K A1 Gordon, William W A1 Wyatt, Brent H A1 White, Peter A1 Marvin, Colby T A1 Helle, Emmi A1 Ojala, Tiina A1 Priest, James R A1 Jenkins, Mary M A1 Almli, Lynn M A1 Reefhuis, Jennita A1 Pangilinan, Faith A1 Brody, Lawrence C A1 McBride, Kim L A1 Garg, Vidu A1 Shaw, Gary M A1 Romitti, Paul A A1 Nembhard, Wendy N A1 Browne, Marilyn L A1 Werler, Martha M A1 Kay, Denise M A1 Mital, Seema A1 Chong, Jessica X A1 Nascone-Yoder, Nanette M A1 Bamshad, Michael J PB Cell Press, Elsevier, Inc. YR 2023 K1 association K1 congenital heart defect K1 development K1 exome sequencing K1 frog K1 oligogenic K1 Xenopus K1 General medicine K1 internal medicine and other clinical medicine K1 Genetics K1 developmental biology K1 physiology JF 10.1016/j.xhgg.2023.100232 LK http://hdl.handle.net/10138/566230 DO http://hdl.handle.net/10138/566230 SF ELIB - SuUB Bremen
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