Resultats de la cerca - Surti, Urvashi

Follicular lymphoma-like B cells of uncertain significance (in situ follicular lymphoma) may infrequently progress, but precedes follicular lymphoma, is associated with other overt... per Pillai, Raju K., Surti, Urvashi, Swerdlow, Steven H.

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Application of Multicolor Banding for Identification of Complex Chromosome 18 Rearrangements per Hu, Jie, Sathanoori, Malini, Kochmar, Sally J., Surti, Urvashi

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Recent advances of genomic testing in perinatal medicine per Peters, David G., Yatsenko, Svetlana A., Surti, Urvashi, Rajkovic, Aleksandar

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Xp11.2 translocation renal cell carcinoma occurring during pregnancy with a novel translocation involving chromosome 19: a case report with review of the literature per Armah, Henry B, Parwani, Anil V, Surti, Urvashi, Bastacky, Sheldon I

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A recurrent translocation is mediated by homologous recombination between HERV-H elements per Hermetz, Karen E, Surti, Urvashi, Cody, Jannine D, Rudd, M Katharine

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Discovery of Epigenetic Biomarkers for the Non-Invasive Diagnosis of Fetal Disease per Bunce, Kimberly, Chu, Tianjiao, Surti, Urvashi, Hogge, W. Allen, Peters, David G.

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Structural and Regulatory Characterization of the Placental Epigenome at Its Maternal Interface per Chu, Tianjiao, Handley, Daniel, Bunce, Kimberly, Surti, Urvashi, Hogge, W. Allen, Peters, David G.

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Whole Exome Sequencing in a Random Sample of North American Women with Leiomyomas Identifies MED12 Mutations in Majority of Uterine Leiomyomas per McGuire, Megan M., Yatsenko, Alexander, Hoffner, Lori, Jones, Mirka, Surti, Urvashi, Rajkovic, Aleksandar

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CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders per Hu, Jie, Liao, Jun, Sathanoori, Malini, Kochmar, Sally, Sebastian, Jessica, Yatsenko, Svetlana A., Surti, Urvashi

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Med12 gain-of-function mutation causes leiomyomas and genomic instability per Mittal, Priya, Shin, Yong-hyun, Yatsenko, Svetlana A., Castro, Carlos A., Surti, Urvashi, Rajkovic, Aleksandar

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Recurrent Triploid and Dispermic Conceptions in Patients with NLRP7 Mutations per Slim, Rima, Ao, Asangla, Surti, Urvashi, Zhang, Li, Hoffner, Lori, Arseneau, Jocelyne, Cheung, Annie, Chebaro, Wafaa, Wischmeijer, Anita

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Chromosome 12q13.13q13.13 microduplication and microdeletion: a case report and literature review per Hu, Jie, Ou, Zhishuo, Infante, Elena, Kochmar, Sally J., Madan-Khetarpal, Suneeta, Hoffner, Lori, Parsazad, Shafagh, Surti, Urvashi

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Follicular lymphomas with plasmacytic differentiation include two subtypes per Gradowski, Joel F, Jaffe, Elaine S, Warnke, Roger A, Pittaluga, Stefania, Surti, Urvashi, Gole, Leena A, Swerdlow, Steven H

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Three Supernumerary Marker Chromosomes in a Patient with Developmental Delay, Mental Retardation, and Dysmorphic Features per Hu, Jie, Madan-Khetarpal, Suneeta, Serrano Russi, Alvaro H., Kochmar, Sally, DeWard, Stephanie J., Sathanoori, Malini, Surti, Urvashi

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Reassessment of small lymphocytic lymphoma in the era of monoclonal B-cell lymphocytosis per Gibson, Sarah E., Swerdlow, Steven H., Ferry, Judith A., Surti, Urvashi, Dal Cin, Paola, Harris, Nancy Lee, Hasserjian, Robert P.

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Chondromyxoid fibroma of rib with a novel chromosomal translocation: a report of four additional cases at unusual sites per Armah, Henry B, McGough, Richard L, Goodman, Mark A, Gollin, Susanne M, Surti, Urvashi, Parwani, Anil V, Rao, Uma NM

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Expression and trafficking of placental microRNAs at the feto-maternal interface per Chang, Guojing, Mouillet, Jean-François, Mishima, Takuya, Chu, Tianjiao, Sadovsky, Elena, Coyne, Carolyn B., Parks, W. Tony, Surti, Urvashi, Sadovsky, Yoel

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Noninvasive Prenatal Diagnosis of a Fetal Microdeletion Syndrome per Peters, David, Chu, Tianjiao, Yatsenko, Svetlana A., Hendrix, Nancy, Hogge, W. Allen, Surti, Urvashi, Bunce, Kimberly, Dunkel, Mary, Shaw, Patricia, Rajkovic, Aleksandar

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Molecular and Clinical Characterization of a Recurrent Cryptic Unbalanced t(4q;18q) Resulting in an 18q Deletion and 4q Duplication. per Horbinski, Craig, Carter, Erika M., Heard, Patricia L., Sathanoori, Malini, Hu, Jie, Vockley, Jerry, Gunn, Shelly, Hale, Daniel E., Surti, Urvashi, Cody, Jannine D.

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Intestinal γδ T-cell lymphomas are most frequently of type II enteropathy-associated T-cell type per Wilson, Amanda L., Swerdlow, Steven H., Przybylski, Grzegorz K., Surti, Urvashi, Choi, John K., Campo, Elias, Trucco, Massimo M., Van Oss, S. Branden, Felgar, Raymond E.

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