Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay von Burnside, Rachel D., Pasion, Romela, Mikhail, Fady M., Carroll, Andrew J., Robin, Nathaniel H., Youngs, Erin L., Gadi, Inder K., Keitges, Elizabeth, Jaswaney, Vikram L., Papenhausen, Peter R., Potluri, Venkateswara R., Risheg, Hiba, Rush, Brooke, Smith, Janice L., Schwartz, Stuart, Tepperberg, James H., Butler, Merlin G.

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Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy von Rudd, M. Katharine, Schleede, Justin B., Williams, Sabrina R., Lee, Kristy, Laffin, Jennifer, Pasion, Romela, Papenhausen, Peter R.

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Expression of the Bs2 pepper gene confers resistance to bacterial spot disease in tomato von Tai, T.H, Dahlbeck, D, Clark, E.T, Gajiwala, P, Pasion, R, Whalen, M.C, Stall, R.E, Staskawicz, B.J

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Clinical Comparison of Overlapping Deletions of 19p13.3 von Risheg, Hiba, Pasion, Romela, Sacharow, Stephanie, Proud, Virginia, Immken, LaDonna, Schwartz, Stuart, Tepperberg, Jim H., Papenhausen, Peter, Tan, Tiong Y., Andrieux, Joris, Plessis, Ghislaine, Amor, David J., Keitges, Elisabeth A.

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Congenital disorder of glycosylation Ic due to a de novo deletion and an hALG-6 mutation von Eklund, Erik A, Sun, Liangwu, Yang, Samuel P, Pasion, Romela M, Thorland, Erik C, Freeze, Hudson H

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UPD detection using homozygosity profiling with a SNP genotyping microarray von Papenhausen, Peter, Schwartz, Stuart, Risheg, Hiba, Keitges, Elisabeth, Gadi, Inder, Burnside, Rachel D., Jaswaney, Vikram, Pappas, John, Pasion, Romela, Friedman, Kenneth, Tepperberg, James

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PATH-45. CLINICAL UTILITY OF COMBINED NEXT GENERATION SEQUENCING AND CHROMOSOMAL MICROARRAY ANALYSIS FOR THE DIAGNOSIS AND MANAGEMENT OF ADULT GLIOMAS von Praska, Corinne, Kollmeyer, Thomas, Fritcher, Emily Barr, Voss, Jesse, McKenna, Michelle, Balcom, Jessica, Pryzbylski, Amber, Pasion, Romela, Kipp, Benjamin, Raghunathan, Aditya, Vaubel, Rachael, Passow, Jeanette Eckel, Lachance, Daniel, Ida, Cristiane, Giannini, Caterina, Jenkins, Robert

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80: Chromosomal microarray analysis of over 45,000 prenatal patients: Significance and efficacy as a first tier diagnostic test von Schwartz, Stuart, Pasion, Romela, Cabral, Huong, Burnside, Rachel, Gadi, Inder, Phillips, Karen, Rudd, Mary K., Schleede, Justin, Tepperberg, James, Papenhausen, Peter

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1 - Direct FISH, Cultured Chromosome Analysis, and Direct SNP Microarray Analysis in Identifying Ring Chromosomes on Prenatal Analysis: A Case of 45,X/46,X,r(X) von Risheg, Hiba, Tepperberg, Jim, Pasion, Romela, Starkey, Elizabeth, Lubben, Briana, Neufeld-Kaiser, Whitney, Liu, Yajuan J.

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Prenatal diagnosis of two fetuses with deletions of 8p23.1, critical region for congenital diaphragmatic hernia and heart defects von Keitges, Elisabeth A., Pasion, Romela, Burnside, Rachel D., Mason, Carla, Gonzalez-Ruiz, Antonio, Dunn, Teresa, Masiello, Meredith, Gebbia, Joseph A., Fernandez, Carlos O., Risheg, Hiba

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59 - Prenatal SNP Microarray Analysis and Parental Follow-up of 16q24.1 Deletions That Include the FOXF1 Gene von Schleede, Justin, Papenhausen, Peter, Risheg, Hiba, Phillips, Karen, Pasion, Romela, David, Karen, Manchester, David, Tucker, Bethany, Wymore, Erica, Noorjahan, Ali

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Prenatal SNP Microarray Analysis and Parental Follow-up of 16q24.1 Deletions That Include the FOXF1 Gene von Schleede, Justin, Papenhausen, Peter, Risheg, Hiba, Phillips, Karen, Pasion, Romela, David, Karen, Manchester, David, Tucker, Bethany, Wymore, Erica, Noorjahan, Ali

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Direct FISH, Cultured Chromosome Analysis, and Direct SNP Microarray Analysis in Identifying Ring Chromosomes on Prenatal Analysis: A Case of 45,X/46,X,r(X) von Risheg, Hiba, Tepperberg, Jim, Pasion, Romela, Starkey, Elizabeth, Lubben, Briana, Neufeld-Kaiser, Whitney, Liu, Yajuan J

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Subtelomeric deletion of chromosome 10p15.3: Clinical findings and molecular cytogenetic characterization von DeScipio, Cheryl, Conlin, Laura, Rosenfeld, Jill, Tepperberg, James, Pasion, Romela, Patel, Ankita, McDonald, Marie T., Aradhya, Swaroop, Ho, Darlene, Goldstein, Jennifer, McGuire, Marianne, Mulchandani, Surabhi, Medne, Livija, Rupps, Rosemarie, Serrano, Alvaro H., Thorland, Erik C., Tsai, Anne C.-H., Hilhorst-Hofstee, Yvonne, Ruivenkamp, Claudia A.L., Van Esch, Hilde, Addor, Marie-Claude, Martinet, Danielle, Mason, Thornton B.A., Clark, Dinah, Spinner, Nancy B., Krantz, Ian D.

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Incidental Findings Found in Whole Genome SNP Microarray Analysis in Both Prenatal and Oncology Studies von Schwartz, Stuart, Pasion, Romela, Cabral, Huong, Gadi, Inder, Jaswaney, Vik, Penton, Andrea, Phillips, Karen, Kline, Laura, Molinari, Sharon, Johansen, Margriet, Shafer, Jenny, Burnside, Rachel D, Tepperberg, James, Williford, Brian, Papenhausen, Peter

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13 - Incidental Findings Found in Whole Genome SNP Microarray Analysis in Both Prenatal and Oncology Studies von Schwartz, Stuart, Pasion, Romela, Cabral, Huong, Gadi, Inder, Jaswaney, Vik, Penton, Andrea, Phillips, Karen, Kline, Laura, Molinari, Sharon, Johansen, Margriet, Shafer, Jenny, Burnside, Rachel D., Tepperberg, James, Williford, Brian, Papenhausen, Peter

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Subtelomeric deletion of chromosome 10p15.3: Clinical findings and molecular cytogenetic characterization von Descipio, Cheryl, Conlin, Laura, Rosenfeld, Jill, Tepperberg, James, Pasion, Romela, Patel, Ankita, McDonald, Marie T, Aradhya, Swaroop, Goldstein, Jennifer, McGuire, Marianne, Mulchandani, Surabhi, Medne, Livija, Rupps, Rosemarie, Serrano, Alvaro H, Thorland, Erik C, Tsai, Anne C.-H, Hilhorst-Hofstee, Yvonne, Ruivenkamp, Claudia A.L, Van Esch, Hilde, Addor, Marie-Claude, Martinet, Danielle, Mason, Thornton B.A, Clark, Dinah, Spinner, Nancy B, Krantz, Ian D

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Congenital disorder of glycosylation Ic due to a de novo deletion and an h ALG-6 mutation von Eklund, Erik A., Sun, Liangwu, Yang, Samuel P., Pasion, Romela M., Thorland, Erik C., Freeze, Hudson H.

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