المؤلفون: Celestino-Soper Patrícia BS, Skinner Cindy, Schroer Richard, Eng Patricia, Shenai Jayant, Nowaczyk Malgorzata MJ, Terespolsky Deborah, Cushing Donna, Patel Gayle S, Immken LaDonna, Willis Alecia, Wiszniewska Joanna, Matalon Reuben, Rosenfeld Jill A, Stevenson Roger E, Kang Sung-Hae L, Cheung Sau, Beaudet Arthur L, Stankiewicz Pawel

المصدر: Molecular Cytogenetics, Vol 5, Iss 1, p 17 (2012)

مصطلحات موضوعية: 6p deletions, Copy-number variants, Array comparative genomic hybridization, Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: http://www.molecularcytogenetics.org/content/5/1/17Test; https://doaj.org/toc/1755-8166Test

الوصول الحر: https://doaj.org/article/6b33cf3605f24009b5cbbc295234f8e2Test

المؤلفون: Eng, Patricia Mona, Kawachi, Ichiro, Fitzmaurice, Garrett, Rimm, Eric B.

المصدر: Journal of Epidemiology and Community Health (1979-), 2005 Jan 01. 59(1), 56-62.

الوصول الحر: https://www.jstor.org/stable/25570610Test

المؤلفون: Eng, Patricia Mona

المصدر: Pleiades: Literature in Context; May 2024, Vol. 44 Issue: 1 p83-83, 1p

المؤلفون: Corney, Paul, Collison, Chris, Eng, Patricia

المصدر: Refer; Spring2019, Vol. 35 Issue 2, p15-21, 7p

المؤلفون: Schaaf, Christian P, Boone, Philip M, Sampath, Srirangan, Williams, Charles, Bader, Patricia I, Mueller, Jennifer M, Shchelochkov, Oleg A, Brown, Chester W, Crawford, Heather P, Phalen, James A, Tartaglia, Nicole R, Evans, Patricia, Campbell, William M, Chun-Hui Tsai, Anne, Parsley, Lea, Grayson, Stephanie W, Scheuerle, Angela, Luzzi, Carol D, Thomas, Sandra K, Eng, Patricia A

المصدر: European Journal of Human Genetics; Dec2012, Vol. 20 Issue 12, p1240-1247, 8p, 1 Diagram, 3 Charts, 1 Graph

مصطلحات موضوعية: PHENOTYPES, EXONS (Genetics), DELETION mutation, DEVELOPMENTAL disabilities, NEUREXINS, HUMAN abnormalities, SPASMS, PATIENTS

المؤلفون: Mona Eng, Patricia, Mast, T. Christopher, Loughlin, Jeanne, Clifford, C. Robin, Wong, Judy, Seeger, John D.

المصدر: Pediatric Infectious Disease Journal; Mar2012, Vol. 31 Issue 3, p287-291, 5p

المؤلفون: Liu, Pengfei, Erez, Ayelet, Sreenath Nagamani, Sandesh C., Bi, Weimin, Carvalho, Claudia M. B., Simmons, Alexandra D., Wiszniewska, Joanna, Fang, Ping, Eng, Patricia A., Cooper, M. Lance, Sutton, V. Reid, Roeder, Elizabeth R., Bodensteiner, John B., Delgado, Mauricio R., Prakash, Siddharth K., Belmont, John W., Stankiewicz, Pawel, Berg, Jonathan S., Shinawi, Marwan, Patel, Ankita

المصدر: Human Molecular Genetics; May2011, Vol. 20 Issue 10, p1975-1988, 14p

المؤلفون: Nagamani, Sandesh C. Sreenath, Erez, Ayelet, Bader, Patricia, Lalani, Seema R., Scott, Daryl A., Scaglia, Fernando, Plon, Sharon E., Chun-Hui Tsai, Reimschisel, Tyler, Roeder, Elizabeth, Malphrus, Amy D., Eng, Patricia A., Hixson, Patricia M., Kang, Sung-Hae L., Stankiewicz, Pawel, Patel, Ankita, Sau Wai Cheung

المصدر: European Journal of Human Genetics; Mar2011, Vol. 19 Issue 3, p280-286, 7p, 2 Diagrams, 3 Charts

مصطلحات موضوعية: HUMAN behavior, PHENOTYPES, COMPARATIVE genomic hybridization, JOINT hypermobility, CRANIOSYNOSTOSES, CHROMOSOMES, POLYDACTYLY, GENETICS

المؤلفون: Boone, Philip M., Bacino, Carlos A., Shaw, Chad A., Eng, Patricia A., Hixson, Patricia M., Pursley, Amber N., Kang, Sung-Hae L., Yang, Yaping, Wiszniewska, Joanna, Nowakowska, Beata A., del Gaudio, Daniela, Xia, Zhilian, Simpson-Patel, Gayle, Immken, LaDonna L., Gibson, James B., Tsai, Anne C.-H., Bowers, Jennifer A., Reimschisel, Tyler E., Schaaf, Christian P., Potocki, Lorraine

المصدر: Human Mutation; Dec2010, Vol. 31 Issue 12, p1326-1342, 17p