Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Dorit Berlin"'
Autor:
Laura B. Scheinfeldt, Kelly Hodges, Jonathan Pevsner, Dorit Berlin, Nahid Turan, Norman P. Gerry
Publikováno v:
BMC Research Notes, Vol 11, Iss 1, Pp 1-5 (2018)
Abstract Objective Lymphoblastoid cell lines are widely used in genetic and genomic studies. Previous work has characterized variant stability in transformed culture and across culture passages. Our objective was to extend this work to evaluate singl
Externí odkaz:
https://doaj.org/article/2917e2133b864ea4a16ec0be0fae9478
Autor:
Jennifer Garbarini, Dianne Gallagher, Meghan K Mac Neal, Michelle Olive, Josée Dupuis, Emma Marquez, Jessica Tusi, Bruce D. Gelb, Mike Italia, Laura E. Mitchell, Roger E. Breitbart, Elaine Mardis, Lynn A. Sleeper, Gail D. Pearson, Nhu Tran, Cassie Mintz, Elizabeth Goldmuntz, Rosalind Korsin, Kristin E. Burns, Joel H. Saltz, Inga Peter, Denise Guevara, Stacy Woyciechowski, Howard S. Seiden, Hakon Hakonarson, Christine Beiswanger, Hector R. Wong, Steven D. Colan, Kimberly Dandreo, James Bristow, Davina Etwaru, Ellen Rosenberg, Ariel Julian, Jeffrey Botkin, George A. Porter, Richard B. Kim, Jennie Kline, Peter White, Christina Kendziorski, Barbara McDonough, Ismee A. Williams, Nancy Stellato, Ravi Sachidanandam, Clinical Sites, Vidu Garg, Minmin Lu, Katrina Celia, John E. Deanfield, Charlene Schramm, Dorothy Warburton, Juan Pablo Kaski, Amy E. Roberts, Maria M. Brooks, Abigail Wilpers, Martina Brueckner, Christine E. Seidman, Alyssa Lanz, Jeffrey C. Murray, Dorit Berlin, Jonathan R. Kaltman, Todd Evans, Judith Geva, Karen Flack, Sharon Edman, Angela Monafo, Jane Newburger, Jonathan G. Seidman, Angela Romano-Adesman, Eileen Taillie, Laura Mercer-Rosa, Janice Stryker, Jaswinder Kaur Sond, Nancy Cross, Sharon Tennstedt, Roslyn Yee, Michael S. Watson, Danielle Awad, Dorota Gruber, Richard P. Lifton, Alessandro Giardini, Wendy K. Chung
Publikováno v:
Circulation research. 112(4)
Congenital heart defects (CHD) are the leading cause of infant mortality among birth defects, and later morbidities and premature mortality remain problematic. Although genetic factors contribute significantly to cause CHD, specific genetic lesions a