Zobrazeno 1 - 7 of 7 pro vyhledávání: '"Mary K. Travis"'
1
ACOG and SMFM guidelines for prenatal diagnosis: Is karyotyping really sufficient?
Autor: Natasa Dzidic, Karine Hovanes, Michelle N. Strecker, Trilochan Sahoo, Sara B. Hay, Charles Doherty, Mary K. Travis
Publikováno v: Prenatal Diagnosis
What's already known about this topic? Current professional guidelines regarding the use of chromosomal microarray analysis (CMA) versus karyotyping in prenatal diagnosis support CMA over karyotype only when fetal structural abnormalities are present
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12793bc23d8ca0cba2c45aa42b421cd1
http://europepmc.org/articles/PMC5900922
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3
Ovarian cancer risk factors by tumor aggressiveness: An analysis from the Ovarian Cancer Cohort Consortium
Autor: Fortner, Renee T. Poole, Elizabeth M. Wentzensen, Nicolas A. and Trabert, Britton White, Emily Arslan, Alan A. Patel, V, Alpa and Setiawan, V. Wendy Visvanathan, Kala Weiderpass, Elisabete and Adami, Hans-Olov Black, Amanda Bernstein, Leslie and Brinton, Louise A. Buring, Julie Clendenen, V, Tess and Fournier, Agnes Fraser, Gary Gapstur, Susan M. Gaudet, Mia M. Giles, Graham G. Gram, Inger T. Hartge, Patricia and Hoffman-Bolton, Judith Idahl, Annika Kaaks, Rudolf Kirsh, Victoria A. Knutsen, Synnove Koh, Woon-Puay Lacey, Jr., James V. Lee, I-Min Lundin, Eva Merritt, Melissa A. and Milne, Roger L. Onland-Moret, N. Charlotte Peters, Ulrike and Poynter, Jenny N. Rinaldi, Sabina Robien, Kim Rohan, Thomas and Sanchez, Maria-Jose Schairer, Catherine Schouten, Leo J. and Tjonneland, Anne Townsend, Mary K. Travis, Ruth C. and Trichopoulou, Antonia van den Brandt, Piet A. Vineis, Paolo and Wilkens, Lynne Wolk, Alicja Yang, Hannah P. and Zeleniuch-Jacquotte, Anne Tworoger, Shelley S.
Ovarian cancer risk factors differ by histotype; however, within subtype, there is substantial variability in outcomes. We hypothesized that risk factor profiles may influence tumor aggressiveness, defined by time between diagnosis and death, indepen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::7bd9e2f64c35795090caf538665b0257
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3184781
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5
Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges
Autor: Natasa Dzidic, Craig A. Dise, Mary K. Travis, Trilochan Sahoo, Charles Doherty, Sara Commander, Carlos W. Benito, Michelle N. Strecker, Karine Hovanes, R. Weslie Tyson, Mandolin S. Ziadie, Arturo E. Mendoza, Mary D. Stephenson
Publikováno v: Genetics in medicine : official journal of the American College of Medical Genetics. 19(1)
Chromosomal microarray analysis (CMA) is currently considered first-tier testing in pediatric care and prenatal diagnosis owing to its high diagnostic sensitivity for chromosomal imbalances. The aim of this study was to determine the efficacy and dia
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ced792e048c75fc7d5829533dcdbc60d
https://pubmed.ncbi.nlm.nih.gov/27337029
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6
Expanding noninvasive prenatal testing to include microdeletions and segmental aneuploidy: cause for concern?
Autor: Michelle N. Strecker, Karine Hovanes, Trilochan Sahoo, Mary K. Travis, Natasa Dzidic, Sara Commander
Publikováno v: Genetics in medicine : official journal of the American College of Medical Genetics. 18(3)
Expanding noninvasive prenatal testing to include microdeletions and segmental aneuploidy: cause for concern?
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80f6ba4298ee98000641198f1c95f9da
https://pubmed.ncbi.nlm.nih.gov/26795591
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