Mammary analog secretory carcinoma, low-grade salivary duct carcinoma, and mimickers: a comparative study von Stevens, Todd M, Kovalovsky, Andra O, Velosa, Claudia, Shi, Qiuying, Dai, Qian, Owen, Randall P, Bell, Walter C, Wei, Shi, Althof, Pamela A, Sanmann, Jennifer N, Sweeny, Larissa, Carroll, William R, Siegal, Gene P, Bullock, Martin J, Brandwein-Gensler, Margaret

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ALK-positive Large B-cell Lymphoma: A Clinicopathologic Study of 26 Cases With Review of Additional 108 Cases in the Literature von Pan, Zenggang, Hu, Shimin, Li, Min, Zhou, Yi, Kim, Young S, Reddy, Vishnu, Sanmann, Jennifer N, Smith, Lynette M, Chen, Mingyi, Gao, Zifen, Wang, Huan-You, Yuan, Ji

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High‐risk cytogenetics in multiple myeloma: Further scrutiny of deletions within the IGH gene region enhances risk stratification von Smith, Scott C., Althof, Pamela A., Dave, Bhavana J., Sanmann, Jennifer N.

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The QT Interval in Patients With the Turner Syndrome von Harrahill, Noah J., Yetman, Anji T., Danford, David A., Starr, Lois J., Sanmann, Jennifer N., Robinson, Jeffrey A.

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Lymphomas with pseudo–double-hit BCL6-MYC translocations due to t(3;8)(q27;q24) are associated with a germinal center immunophenotype, extranodal involvement, and frequent BCL2 tra... von Johnson, Steven M., Umakanthan, Jayadev Manikkam, Yuan, Ji, Fedoriw, Yuri, Bociek, R. Gregory, Kaiser-Rogers, Kathleen, Sanmann, Jennifer N., Montgomery, Nathan D.

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Additional comments regarding IGH studies in multiple myeloma von Smith, Scott C., Althof, Pamela A., Dave, Bhavana J., Sanmann, Jennifer N.

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The recurrent TUBB3 Gly98Ser substitution is the first described to inconsistently result in CFEOM3 von Smith, Scott C., Olney, Ann Haskins, Beavers, Angela, Spaulding, Joanna, Nelson, Marilu, Nielsen, Shelly, Sanmann, Jennifer N.

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Vascular dissection in women with Turner syndrome von Yetman, Anji T., Bisselou, Karl Stessy M., Sanmann, Jennifer N., Katz, Renee J., Steingraeber, Catherine J., Wilde, Megan, Murray, Mary, Starr, Lois J.

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A novel MYC–non‐IG fusion in refractory diffuse large B‐cell lymphoma von Wang, Cheng, Althof, Pamela A., Bi, Chengfeng, Zhang, Weiwei, Bouska, Alyssa C., Tian, Tian, Zhang, Xuan, Jiang, Nanxi, Yu, Guohua, Cheng, Hongxia, Iqbal, Javeed, Vose, Julie M., Sanmann, Jennifer N., Fu, Kai

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A Val66Met polymorphism is associated with weaker somatosensory cortical activity in individuals with cerebral palsy von Trevarrow, Michael, Sanmann, Jennifer N., Wilson, Tony W., Kurz, Max J.

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Myhre syndrome: Clinical features and restrictive cardiopulmonary complications von Starr, Lois J., Grange, Dorothy K., Delaney, Jeffrey W., Yetman, Anji T., Hammel, James M., Sanmann, Jennifer N., Perry, Deborah A., Schaefer, G. Bradley, Olney, Ann Haskins

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MECOM rearrangement involving the MYC locus: Two additional patients with the rare translocation, t(3;8)(q26.2;q24), and molecular review von Smith, Scott C., Qdaisat, Tareq Z.S., Althof, Pamela A., Dave, Bhavana J., Sanmann, Jennifer N.

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Frequency, variations, and prognostic implications of chromosome 14q32 deletions in chronic lymphocytic leukemia von Harris, Rachel A., Stevens, Jadd. M., Pickering, Diane L., Althof, Pamela A., Smith, Lynette M., Sanmann, Jennifer N., Dave, Bhavana J.

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Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar von Riggs, Erin R., Nelson, Tristan, Merz, Andrew, Ackley, Todd, Bunke, Brian, Collins, Christin D., Collinson, Morag N., Fan, Yao‐Shan, Goodenberger, McKinsey L., Golden, Denae M., Haglund‐Hazy, Linda, Krgovic, Danijela, Lamb, Allen N., Lewis, Zoe, Li, Guang, Liu, Yajuan, Meck, Jeanne, Neufeld‐Kaiser, Whitney, Runke, Cassandra K., Sanmann, Jennifer N., Stavropoulos, Dimitri J., Strong, Emma, Su, Meng, Tayeh, Marwan K., Kokalj Vokac, Nadja, Thorland, Erik C., Andersen, Erica, Martin, Christa L.

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Genome wide copy number analysis of paediatric Burkitt lymphoma using formalin‐fixed tissues reveals a subset with gain of chromosome 13q and corresponding miRNA over expression von Schiffman, Joshua D., Lorimer, Patrick D., Rodic, Vladimir, Jahromi, Mona S., Downie, Jonathan M., Bayerl, Michael G., Sanmann, Jennifer N., Althof, Pamela A., Sanger, Warren G., Barnette, Phillip, Perkins, Sherrie L., Miles, Rodney R.

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Valve-Sparing Root and Total Arch Replacement for Cutis Laxa Aortopathy von Yetman, Anji T., Hammel, James, Sanmann, Jennifer N., Starr, Lois J.

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Val66Met Polymorphism Is Associated with Altered Motor-Related Oscillatory Activity in Youth with Cerebral Palsy von Trevarrow, Michael P, Bergwell, Hannah, Sanmann, Jennifer, Wilson, Tony W, Kurz, Max J

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Mammary analog secretory carcinoma, low-grade salivary duct carcinoma, and mimickers: a comparative study von Stevens, Todd M, Kovalovsky, Andra O, Velosa, Claudia, Shi, Qiuying, Dai, Qian, Owen, Randall P, Bell, Walter C, Wei, Shi, Althof, Pamela A, Sanmann, Jennifer N, Sweeny, Larissa, Carroll, William R, Siegal, Gene P, Bullock, Martin J, Brandwein-Gensler, Margaret

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Assessing the utility of confirmatory studies following identification of large-scale genomic imbalances by microarray von Sanmann, Jennifer N., Pickering, Diane L., Golden, Denae M., Stevens, Jadd M., Hempel, Thomas E., Althof, Pamela A., Wiggins, Michele L., Starr, Lois J., Davé, Bhavana J., Sanger, Warren G.

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The first patient with tandem duplication of 6q14q16: Molecular and phenotypic characterization von Sanmann, Jennifer N., Casas, Kari A., Bevilacqua, Jen, Bishay, Danielle L., Clark, Tanner, Van Dyke, A. Zephyr, Leiferman, Patricia Crotwell, Reddi, Honey V., Starr, Lois J.

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