Rezultati pretrage - Catherine Cottrell

Clinically significant findings in a decade‐long retrospective study of prenatal chromosomal microarray testing od Joie O. Olayiwola, Mohammad Marhabaie, Daniel Koboldt, Theodora Matthews, Amy Siemon, Danielle Mouhlas, Taylor Porter, George Kyle, Cortlandt Myers, Hui Mei, Ying‐Chen Claire Hou, Melanie Babcock, Jesse Hunter, Kathleen M. Schieffer, Yassmine Akkari, Shalini Reshmi, Catherine Cottrell, Mariam T. Mathew, Marco L. Leung

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O13: Clinical validation of copy number alteration using paired tumor-normal exome sequencing: Challenges and successes* od Kathleen Schieffer, David Gordon, Gregory Wheeler, Grant Lammi, Don Corsmeier, Douglas Depoorter, Liana Hernandez, Jessica Howard, Vijayakumar Jayaraman, Prasad Kopparapu, Jordan Olberding, Melanie Babcock, Ying-Chen Claire Hou, Marco Leung, Mariam Mathew, Yassmine Akkari, Peter White, Richard Wilson, Elaine Mardis, Catherine Cottrell

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P070: Discerning the meaning of cancer predisposition variants in a pediatric cancer cohort od Erica Macke, Kathleen Schieffer, Mariam Mathew, Marco Leung, Yassmine Akkari, Melanie Babcock, Ying-Chen Claire Hou, Liana Hernandez, Jordan Olberding, Prasad Kopparapu, Vijayakumar Jayaraman, Don Corsmeier, Jessica Howard, Douglas Depoorter, Kristin Zajo, Peter White, Benjamin Kelly, Richard Wilson, Elaine Mardis, Catherine Cottrell

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22: A case of partial trisomy 13 not detected on prenatal cfDNA screen od Laura Bryant, Mari Mori, Bimal P. Chaudhari, Michael Zinmeister, Nathan Johnson, Elizabeth Hamelberg, Kimberly Wetherell, Don Roman, Jeffrey Wobser, Joon Kim, Matthew Meleski, Veronica Reher, Shalini C. Reshmi, Jason P. Garee, Jesse Hunter, Catherine Cottrell, Marco Leung, Taylor Porter, Theodora Matthews, Yassmine Akkari

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O09: Prevalence of germline variants in cancer predisposition genes in patients with pediatric solid tumors using paired tumor-normal exome sequencing od Ying-Chen Claire Hou, Kareesma Parbhoo, Benjamin Kelly, Grant Lammi, Vijayakumar Jayaraman, Don Corsmeier, Douglas Depoorter, Jessica Howard, Liana Hernandez, Jordan Olberding, Amy Everest, Swetha Ramadesikan, Sean Caruthers, Alejandro Otero Bravo, Melanie Babcock, Kathleen Schieffer, Marco Leung, Mariam Mathew, Yassmine Akkari, Elaine Mardis, Catherine Cottrell

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P726: Provenance/identity testing in genome sequencing: A single institution’s experience od Fang Fang, Tessa Gonzalez, Vruti Mehta, Vijayakumar Jayaraman, Don Corsmeier, Aimee McKinney, Heather Jenkins, Spencer Ravagnani, Theodora Matthews, Jason Garee, Benjamin Kelly, Gregory Wheeler, Daniel Koboldt, Melanie Babcock, Vanessa Horner, Kathleen Schieffer, Marco Leung, Mariam Mathew, Ying-Chen Claire Hou, Jesse Hunter, Catherine Cottrell

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P654: Evaluation of the ClinGen/CGC/VICC Oncogenicity Guidelines to support pediatric variant classification workflows od Wesley Goar, Kori Kuzma, Kathryn Stahl, Kyle Voytovich, Mariam Mathew, Erica Macke, Melanie Babcock, Ying-Chen Claire Hou, Liana Hernandez, Jordan Olberding, Prasad Kopparapu, Vijayakumar Jayaraman, Don Corsmeier, Jessica Howard, Douglas Depoorter, Ashley Kubatko, Grant Lammi, Marco Leung, Kathleen Schieffer, Yassmine Akkari, Elaine Mardis, Peter White, Catherine Cottrell, Alex Wagner

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