Temple syndrome resulting from uniparental disomy is undiagnosed by a methylation assay due to low‐level mosaicism for trisomy 14 von Lindgren, Valerie, Cobian, Katherine, Bhat, Gifty

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Anterior Pituitary Aplasia in an Infant with Ring Chromosome 18p Deletion von Shad, Zohra, Lindgren, Valerie, Durrin, Sarah, Chan, Jacqueline, Bellfield, Edward J., Boucher-Berry, Claudia

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To err is human; to follow the SOP divine von Lindgren, Valerie

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Coexistent Systemic Amyloidosis, Multiple Myeloma, and Refractory Anemia with Ringed Sideroblasts in a Previously Untreated Patient von Mehendale, Sangeeta, Patel, Pritesh, Lindgren, Valerie, Rondelli, Damiano, Gaitonde, Sujata

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Initial Misdiagnosis of a Treatment-Related Myeloid Lineage Neoplasm With Tetrasomy 21 von Graf, Oliver, Patel, Pritesh, Lindgren, Valerie, Gaitonde, Sujata

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Acute myelogenous leukemia with t(6;9)(p23;q34) and marrow basophilia: an overview von Chi, Yiqing, Lindgren, Valerie, Quigley, Sean, Gaitonde, Sujata

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Thrombocytopenia and Predisposition to Acute Myeloid Leukemia due to Mosaic Ring 21 with Loss of RUNX1: Cytogenetic and Molecular Characterization von Vormittag-Nocito, Erica, Ni, Hongyu, Schmidt, Mary L., Lindgren, Valerie

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inv(16)/t(16;16) acute myeloid leukemia with non–type A CBFB-MYH11 fusions associate with distinct clinical and genetic features and lack KIT mutations von Schwind, Sebastian, Edwards, Colin G., Nicolet, Deedra, Mrózek, Krzysztof, Maharry, Kati, Wu, Yue-Zhong, Paschka, Peter, Eisfeld, Ann-Kathrin, Hoellerbauer, Pia, Becker, Heiko, Metzeler, Klaus H., Curfman, John, Kohlschmidt, Jessica, Prior, Thomas W., Kolitz, Jonathan E., Blum, William, Pettenati, Mark J., Dal Cin, Paola, Carroll, Andrew J., Caligiuri, Michael A., Larson, Richard A., Volinia, Stefano, Marcucci, Guido, Bloomfield, Clara D.

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Transition of Long standing JAK2V617F Positive Post-Polycythemia Vera Myelofibrosis to Chronic Myelogenous Leukemia (BCR-ABL1 Positive): An Unusual Event von Gaitonde, Sujata, Bogard, Agatha, Graf, Oliver, Peace, David, Lindgren, Valerie, Mehendale, Sangeeta

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Autism or atypical autism in maternally but not paternally derived proximal 15q duplication von COOK, E. H, LINDGREN, V, LEVENTHAL, B. L, COURCHESNE, R, LINCOLN, A, SHULMAN, C, LORD, C, COURCHESNES, E

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Evaluation of Genotoxicity of Chromatin Modifying Agents Expanded Hematopoietic Graft in a Non-Human Primate Model von Taioli, Simona, Petro, Benjamin, Gaitonde, Sujata, Quigley, John G., Lindgren, Valerie, Borce, Manuel, Sweiss, Karen, Rondelli, Damiano, Mahmud, Nadim

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Unique immunologic patterns in fibromyalgia von Behm, Frederick G, Gavin, Igor M, Karpenko, Oleksiy, Lindgren, Valerie, Gaitonde, Sujata, Gashkoff, Peter A, Gillis, Bruce S

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Effects of chromatin-modifying agents on CD34+ cells from patients with idiopathic myelofibrosis von JUN SHI, YAN ZHAO, ISHII, Takefumi, WENYANG HU, SOZER, Selcuk, WEI ZHANG, BRUNO, Edward, LINDGREN, Valerie, MINGJIANG XU, HOFFMAN, Ronald

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Possible Epigenetic Regulation of Functionally Opposing Groups of Genes Involved in Ex Vivo Expansion of Cord Blood Stem Cells von Baluchamy, Sudhakar, Petro, Benjamin, Araki, Hiroto, Lindgren, Valerie, Mahmud, Nadim

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Behavioral abnormalities are common and severe in patients with distal 22q11.2 microdeletions and microduplications von Lindgren, Valerie, McRae, Anne, Dineen, Richard, Saulsberry, Alexandria, Hoganson, George, Schrift, Michael

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The Principles of Clinical Cytogenetics von Lindgren, Valerie

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Durable complete remission induced by cetuximab monotherapy in a patient infected with HIV and diagnosed with recurrent squamous cell carcinoma of the head and neck von Rubinstein, Paul G, Lindgren, Valerie, Setty, Suman, Yao, Mike, Pytynia, Kristen B, Radosevich, James A, Kadkol, ShriHari S, Feldman, Lawrence E

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The constitutive mobilization of bone marrow-repopulating cells into the peripheral blood in idiopathic myelofibrosis von Xu, Mingjiang, Bruno, Edward, Chao, Joseph, Ni, Hongyu, Lindgren, Valerie, Nunez, Rafael, Mahmud, Nadim, Finazzi, Guido, Fruchtman, Steven M., Popat, Uday, Liu, Enli, Prchal, Josef T., Rondelli, Damiano, Barosi, Giovanni, Hoffman, Ronald

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High incidence of chromosome 1 abnormalities in a series of 27 renal oncocytomas: cytogenetic and fluorescence in situ hybridization studies von Paner, Gladell P, Lindgren, Valerie, Jacobson, Kris, Harrison, Kathleen, Cao, Ying, Campbell, Steve C, Flanigan, Robert C, Picken, Maria M

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Characterization of Ex Vivo Expanded Cord Blood Graft Treated with Chromatin Modifying Agents for Potential Clinical Use von Yoshinaga, Kazumi, Mahmud, Dolores, Baluchamy, Sudhakar, Parajuli, Ritesh, Hiroto, Araki, Lindgren, Valerie, Rondelli, Damiano, Mahmud, Nadim

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