High Levels of Sample-to-Sample Variation Confound Data Analysis for Non-Invasive Prenatal Screening of Fetal Microdeletions. by Tianjiao Chu, Suveyda Yeniterzi, Svetlana A Yatsenko, Mary Dunkel, Patricia A Shaw, Kimberly D Bunce, David G Peters

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Correction: High Levels of Sample-to-Sample Variation Confound Data Analysis for Non-Invasive Prenatal Screening of Fetal Microdeletions. by Tianjiao Chu, Suveyda Yeniterzi, Svetlana A Yatsenko, Mary Dunkel, Patricia A Shaw, Kimberly D Bunce, David G Peters

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Hormad1 mutation disrupts synaptonemal complex formation, recombination, and chromosome segregation in mammalian meiosis. by Yong-Hyun Shin, Youngsok Choi, Serpil Uckac Erdin, Svetlana A Yatsenko, Malgorzata Kloc, Fang Yang, P Jeremy Wang, Marvin L Meistrich, Aleksandar Rajkovic

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Correction: Mutation Disrupts Synaptonemal Complex Formation, Recombination, and Chromosome Segregation in Mammalian Meiosis. by Yong-Hyun Shin, Youngsok Choi, Serpil Uckac Erdin, Svetlana A. Yatsenko, Malgorzata Kloc, Fang Yang, P. Jeremy Wang, Marvin L. Meistrich, Aleksandar Rajkovic

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Correction: Mu heavy chain disease with MYD88 L265P mutation: An unusual manifestation of lymphoplasmacytic lymphoma by Vandana Baloda, Sarah E. Wheeler, David L. Murray, Mindy C. Kohlhagen, Jeffrey A. Vos, Svetlana A. Yatsenko, Mounzer E. Agha, Miroslav Djokic, Steven H. Swerdlow, Nathanael G. Bailey

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Mu heavy chain disease with MYD88 L265P mutation: an unusual manifestation of lymphoplasmacytic lymphoma by Vandana Baloda, Sarah E. Wheeler, David L. Murray, Mindy C. Kohlhagen, Jeffrey A. VosUPMC, Svetlana A. Yatsenko, Mounzer E. Agha, Miroslav Djokic, Steven H. Swerdlow, Nathanael G. Bailey

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Blue cone monochromacy: visual function and efficacy outcome measures for clinical trials. by Xunda Luo, Artur V Cideciyan, Alessandro Iannaccone, Alejandro J Roman, Lauren C Ditta, Barbara J Jennings, Svetlana A Yatsenko, Rebecca Sheplock, Alexander Sumaroka, Malgorzata Swider, Sharon B Schwartz, Bernd Wissinger, Susanne Kohl, Samuel G Jacobson

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Deletion of conserved non‐coding sequences downstream from NKX2‐1: A novel disease‐causing mechanism for benign hereditary chorea by Jun Liao, Keith A. Coffman, Joseph Locker, Quasar S. Padiath, Bruce Nmezi, Robyn A. Filipink, Jie Hu, Malini Sathanoori, Suneeta Madan‐Khetarpal, Marianne McGuire, Allison Schreiber, Rocio Moran, Neil Friedman, Lori Hoffner, Aleksandar Rajkovic, Svetlana A. Yatsenko, Urvashi Surti

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Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases. by Xinyan Lu, Chad A Shaw, Ankita Patel, Jiangzhen Li, M Lance Cooper, William R Wells, Cathy M Sullivan, Trilochan Sahoo, Svetlana A Yatsenko, Carlos A Bacino, Pawel Stankiewicz, Zhishu Ou, A Craig Chinault, Arthur L Beaudet, James R Lupski, Sau W Cheung, Patricia A Ward

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A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease by Benjamin J. Landis, Lindsey R. Helvaty, Gabrielle C. Geddes, Jiuann‐Huey Ivy Lin, Svetlana A. Yatsenko, Cecilia W. Lo, William L. Border, Stephanie Burns Wechsler, Chaya N. Murali, Mahshid S. Azamian, Seema R. Lalani, Robert B. Hinton, Vidu Garg, Kim L. McBride, Jennelle C. Hodge, Stephanie M. Ware

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