Mechanisms Separating Time-Dependent and True Dose-Rate Effects in Irradiated Bipolar Oxides von Rowsey, N. L., Law, M. E., Schrimpf, R. D., Fleetwood, D. M., Tuttle, B. R., Pantelides, S. T.

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Radiation-Induced Oxide Charge in Low- and High-H 2 Environments von Rowsey, Nicole L, Law, Mark E, Schrimpf, Ronald D, Fleetwood, Daniel M, Tuttle, Blair R, Pantelides, Sokrates T

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Radiation-Induced Oxide Charge in Low- and High-H Environments von Rowsey, Nicole L., Law, Mark E., Schrimpf, Ronald D., Fleetwood, Daniel M., Tuttle, Blair R., Pantelides, Sokrates T.

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A Quantitative Model for ELDRS and Degradation Effects in Irradiated Oxides Based on First Principles Calculations von Rowsey, N. L., Law, M. E., Schrimpf, R. D., Fleetwood, D. M., Tuttle, B. R., Pantelides, S. T.

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A Quantitative Model for ELDRS and rm H 2 Degradation Effects in Irradiated Oxides Based on First Principles Calculations von Rowsey, Nicole L, Law, Mark E, Schrimpf, Ronald D, Fleetwood, Daniel M, Tuttle, Blair R, Pantelides, Sokrates T

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Uniparental disomy of multiple chromosomes in two cases with a complex phenotype von Polonis, Katarzyna, Lopes, Jaime L., Cabral, Huong, Babcock, Holly E., Kline, Laura, Ruiz, Kaylee M., Schwartz, Stuart, Hasadsri, Linda, Rowsey, Ross A., Hoppman, Nicole L.

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False-positive XXY results by interphase FISH in cytogenetically normal XX individuals: two cases highlighting the necessity of additional laboratory follow-up von Ding, Qiliang, Bronson, Abigail L, Byerly, Kyna A, Essendrup, Anna A, Mitchell, Elyse B, Runke, Cassandra K, Rowsey, Ross A, Hoppman, Nicole L

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Most noninvasive prenatal screens failing due to inadequate fetal cell free DNA are negative for trisomy when repeated von Lopes, Jaime L., Lopes, Guilherme S., Enninga, Elizabeth A. L., Kearney, Hutton M., Hoppman, Nicole L., Rowsey, Ross A.

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Limited diagnostic impact of duplications <1 Mb of uncertain clinical significance: a 10-year retrospective analysis of reporting practices at the Mayo Clinic von Marcou, Cherisse A., Pitel, Beth, Hagen, Clinton E., Boczek, Nicole J., Rowsey, Ross A., Baughn, Linda B., Hoppman, Nicole L., Thorland, Erik C., Kearney, Hutton M.

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SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq) von Johnson, Sarah H., Smadbeck, James B., Smoley, Stephanie A., Gaitatzes, Athanasios, Murphy, Stephen J., Harris, Faye R., Drucker, Travis M., Zenka, Roman M., Pitel, Beth A., Rowsey, Ross A., Hoppman, Nicole L., Aypar, Umut, Sukov, William R., Jenkins, Robert B., Feldman, Andrew L., Kearney, Hutton M., Vasmatzis, George

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Clinical Validation of Tagmentation-Based Genome Sequencing for Germline Disorders von Shen, Wei, Sellers, Heidi L., Choate, Lauren A., Stein, Mariam I., Tandale, Pratyush P., Tan, Jiayu, Setlem, Rohit, Sakai, Yuta, Fadra, Numrah, Sosa, Carlos, McClelland, Shawn P., Barnett, Sarah S., Rasmussen, Kristen J., Runke, Cassandra K., Smoley, Stephanie A., Tillmans, Lori S., Marcou, Cherisse A., Rowsey, Ross A., Thorland, Erik C., Boczek, Nicole J., Kearney, Hutton M.

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Improving Single-Nucleotide Polymorphism-Based Fetal Fraction Estimation of Maternal Plasma Circulating Cell-Free DNA Using Bayesian Hierarchical Models von Larson, Nicholas B, Wang, Chen, Na, Jie, Rowsey, Ross A, Highsmith, William Edward, Hoppman, Nicole L, Kocher, Jean-Pierre, Klee, Eric W

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16. Uniparental disomy (UPD) of multiple chromosomes in two cases with a complex phenotype von Polonis, Katarzyna, Lopes, Jaime L., Cabral, Huong, Hasadsri, Linda, Rowsey, Ross A., Hoppman, Nicole L.

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Most Non Invasive Prenatal Screens Failing Due to Inadequate Fetal Cell Free DNA are Negative for Trisomy when Repeated von Lopes, Jaime L., Lopes, Guilherme S., Enninga, Elizabeth Ann L., Kearney, Hutton M., Hoppman, Nicole L., Rowsey, Ross A.

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Characterization of TCF3 rearrangements in pediatric B-lymphoblastic leukemia/lymphoma by mate-pair sequencing (MPseq) identifies complex genomic rearrangements and a novel TCF3/TE... von Rowsey, Ross A., Smoley, Stephanie A., Williamson, Cynthia M., Vasmatzis, George, Smadbeck, James B., Ning, Yi, Greipp, Patricia T., Hoppman, Nicole L., Baughn, Linda B., Ketterling, Rhett P., Peterson, Jess F.

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Detection of a cryptic NUP214/ABL1 gene fusion by mate-pair sequencing (MPseq) in a newly diagnosed case of pediatric T-lymphoblastic leukemia von Peterson, Jess F, Pitel, Beth A, Smoley, Stephanie A, Smadbeck, James B, Johnson, Sarah H, Vasmatzis, George, Koon, Sarah J, Webley, Matthew R, McGrath, Mary, Bayerl, Michael G, Baughn, Linda B, Rowsey, Ross A, Ketterling, Rhett P, Greipp, Patricia T, Hoppman, Nicole L

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Whole-Genome Mate Pair Sequencing Reflex Test to Characterize Chromosome Rearrangements in Hematologic Neoplasia von Baughn, Linda B, Pitel, Beth A, Smoley, Stephanie A., Rustin, Jeannette G, Vasmatzis, George, Johnson, Sarah H, Smadbeck, James, Webley, Matthew, Koon, Sarah J, Rowsey, Ross, Kearney, Hutton, Sukov, William, Ketterling, Rhett P., Geiersbach, Katherine, Van Dyke, Daniel L., Jenkins, Robert, Greipp, Patricia, Thorland, Erik, Hoppman, Nicole, Aypar, Umut

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Getting to Know Your LCRs: Recognizing and Interpreting Atypical CNVs in Recurrent Syndromic Microdeletion/Duplication Regions Mediated by Alternative Low Copy Repeat Elements von Rowsey, Ross A, Aypar, Umut, Baughn, Linda B, Hoppman, Nicole L, Thorland, Erik C, Kearney, Hutton M

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48 - Getting to Know Your LCRs: Recognizing and Interpreting Atypical CNVs in Recurrent Syndromic Microdeletion/Duplication Regions Mediated by Alternative Low Copy Repeat Elements von Rowsey, Ross A., Aypar, Umut, Baughn, Linda B., Hoppman, Nicole L., Thorland, Erik C., Kearney, Hutton M.

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