Resultados da busca - Shago, Mary

13q13.1–q13.2 deletion in tetralogy of Fallot: Clinical report and a literature review por Costain, Gregory, Silversides, Candice K., Marshall, Christian R., Shago, Mary, Costain, Nicholas, Bassett, Anne S.

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An aggressive central giant cell granuloma in a pediatric patient: case report and review of literature por Wang, Yiqiao, Le, Andre, El Demellawy, Dina, Shago, Mary, Odell, Michael, Johnson-Obaseki, Stephanie

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Pediatric fibromyxoid soft tissue tumor with PLAG1 fusion: A novel entity? por Chung, Catherine T., Antonescu, Cristina R., Dickson, Brendan C., Chami, Rose, Marrano, Paula, Fan, Rong, Shago, Mary, Hameed, Meera, Thorner, Paul S.

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Genetic Diversity in Alveolar Soft Part Sarcoma: A Subset Contain Variant Fusion Genes, Highlighting Broader Molecular Kinship with Other MiT Family Tumors por Dickson, Brendan C., T-S Chung, Catherine, Hurlbut, David J., Marrano, Paula, Shago, Mary, Sung, Yun-Shao, Swanson, David, Zhang, Lei, Antonescu, Cristina R.

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Molecular testing prognostic of low risk in epithelioid uveal melanoma in a child por Dimaras, Helen, Parulekar, Manoj Vijay, Kwok, Grace, Simpson, E Rand, Ali, Asim, Halliday, William, Shago, Mary, Harbour, J William, Héon, Elise, Gallie, Brenda L, Chan, Helen S L

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A Common Molecular Mechanism Underlies Two Phenotypically Distinct 17p13.1 Microdeletion Syndromes por Shlien, Adam, Baskin, Berivan, Achatz, Maria Isabel W., Stavropoulos, Dimitrios J., Nichols, Kim E., Hudgins, Louanne, Morel, Chantal F., Adam, Margaret P., Zhukova, Nataliya, Rotin, Lianne, Novokmet, Ana, Druker, Harriet, Shago, Mary, Ray, Peter N., Hainaut, Pierre, Malkin, David

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BI-21 BRAF MUTATION AND CDKN2A DELETIONS DEFINE A CLINICALLY DISTINCT SUBGROUP OF CHILDHOOD SECONDARY HIGH GRADE GLIOMA por Mistry, Matthew, Zhukova, Nataliya, Merico, Daniele, Rakopoulos, Patricia, Krishnatry, Rahul, Shago, Mary, Stavropoulos, Jim, Ray, Peter, Mangerel, Joshua, Remke, Marc, Buczkowicz, Pawel, Ramaswamy, Vijay, Rutka, James, Dirks, Peter, Taylor, Michael, Bouffet, Eric, Malkin, David, Huang, Annie, Hawkins, Cynthia, Tabori, Uri

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LG-01 BRAF MUTATION AND CDKN2A DELETION DEFINE A CLINICALLY DISTINCT SUBGROUP OF CHILDHOOD SECONDARY HIGH-GRADE GLIOMA por Mistry, Matthew, Zhukova, Nataliya, Merico, Daniele, Rakopoulos, Patricia, Krishnatry, Rahul, Shago, Mary, Stavropoulos, Jim, Pole, Jason, Ray, Peter, Remke, Marc, Buczkowicz, Pawel, Ramaswamy, Vijay, Shlien, Adam, Rutka, James, Dirks, Peter, Taylor, Michael, Malkin, David, Bouffet, Eric, Hawkins, Cynthia, Tabori, Uri

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Genome assembly comparison identifies structural variants in the human genome por Khaja, Razi, Zhang, Junjun, MacDonald, Jeffrey R, He, Yongshu, Joseph-George, Ann M, Wei, John, Rafiq, Muhammad A, Qian, Cheng, Shago, Mary, Pantano, Lorena, Aburatani, Hiroyuki, Jones, Keith, Redon, Richard, Hurles, Matthew, Armengol, Lluis, Estivill, Xavier, Mural, Richard J, Lee, Charles, Scherer, Stephen W, Feuk, Lars

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SMARCAL1 Deficiency Predisposes to Non-Hodgkin Lymphoma and Hypersensitivity to Genotoxic Agents In vivo por Baradaran-Heravi, Alireza, Raams, Anja, Lubieniecka, Joanna, Cho, Kyoung Sang, DeHaai, Kristi A., Basiratnia, Mitra, Mari, Pierre-Olivier, Xue, Yutong, Rauth, Michael, Olney, Ann Haskins, Shago, Mary, Choi, Kunho, Weksberg, Rosanna A., Nowaczyk, Malgorzata J.M., Wang, Weidong, Jaspers, Nicolaas G.J., Boerkoel, Cornelius F.

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The impact of category, cytopathology and cytogenetics on development and progression of clonal and malignant myeloid transformation in inherited bone marrow failure syndromes por Cada, Michaela, Segbefia, Catherin I., Klaassen, Robert, Fernandez, Conrad V., Yanofsky, Rochelle A., Wu, John, Pastore, Yves, Silva, Mariana, Lipton, Jeffrey H., Brossard, Josee, Michon, Bruno, Abish, Sharon, Steele, MacGregor, Sinha, Roona, Belletrutti, Mark, Breakey, Vicky, Jardine, Lawrence, Goodyear, Lisa, Sung, Lillian, Shago, Mary, Beyene, Joseph, Sharma, Preeti, Zlateska, Bozana, Dror, Yigal

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INNV-43. MORE THAN WHAT MEETS THE EYE: ETMR AN UNDER RECOGNISED ATYPICAL BRAINSTEM PRIMARY. A RARE BRAIN TUMOR CONSORTIUM (RBTC) STUDY por Khan, Sara, Solano-Paez, Palma, Hansford, Jordan R, Lu, Mei, Al-karmi, Salma, Leung, Lydia, Plant-Fox, Ashley, Spina, Melina La, Andrew, Eden, Dunham, Christopher, Phillips, Joanna, Ridola, Rita, Sgouros, Spyros, Hazrati, Lili-Naz, Shago, Mary, Hoffman, Lindsey, Hawkins, Cynthia, Bartel, Ute, Mulchay, Jean, Vibhakar, Rajeev, Andre, Nicolas, Bouffet, Eric, Huang, Annie

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Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay por Uddin, Mohammed, Pellecchia, Giovanna, Thiruvahindrapuram, Bhooma, D’Abate, Lia, Merico, Daniele, Chan, Ada, Zarrei, Mehdi, Tammimies, Kristiina, Walker, Susan, Gazzellone, Matthew J., Nalpathamkalam, Thomas, Yuen, Ryan K. C., Devriendt, Koenraad, Mathonnet, Géraldine, Lemyre, Emmanuelle, Nizard, Sonia, Shago, Mary, Joseph-George, Ann M., Noor, Abdul, Carter, Melissa T., Yoon, Grace, Kannu, Peter, Tihy, Frédérique, Thorland, Erik C., Marshall, Christian R., Buchanan, Janet A., Speevak, Marsha, Stavropoulos, Dimitri J., Scherer, Stephen W.

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The clinical impact of copy number variants in inherited bone marrow failure syndromes por Waespe, Nicolas, Dhanraj, Santhosh, Wahala, Manju, Tsangaris, Elena, Enbar, Tom, Zlateska, Bozana, Li, Hongbing, Klaassen, Robert J., Fernandez, Conrad V., Cuvelier, Geoff D. E., Wu, John K., Pastore, Yves D., Silva, Mariana, Lipton, Jeffrey H., Brossard, Joseé, Michon, Bruno, Abish, Sharon, Steele, MacGregor, Sinha, Roona, Belletrutti, Mark J., Breakey, Vicky R., Jardine, Lawrence, Goodyear, Lisa, Kofler, Liat, Cada, Michaela, Sung, Lillian, Shago, Mary, Scherer, Stephen W., Dror, Yigal

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Masked hypodiploidy: hypodiploid acute lymphoblastic leukemia (ALL) mimicking hyperdiploid ALL in children: A report from the Children’s Oncology Group por Carroll, Andrew J, Shago, Mary, Mikhail, Fady M, Raimondi, Susana C, Hirsch, Betsy A, Loh, Mignon L, Raetz, Elizabeth A, Borowitz, Michael J, Wood, Brent L, Maloney, Kelly W, Mattano, Leonard A, Larsen, Eric C, Gastier-Foster, Julie, Stonerock, Eileen, Ell, Denise, Kahwash, Samir, Devidas, Meenakshi, Harvey, Richard C, Chen, I-Ming L, Willman, Cheryl L, Hunger, Stephen P, Winick, Naomi J, Carroll, William L, Rao, Kathleen W, Heerema, Nyla A

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Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome por McQuaid, Mary E., Ahmed, Kashif, Tran, Stephanie, Rousseau, Justine, Shaheen, Ranad, Kernohan, Kristin D., Yuki, Kyoko E., Grover, Prerna, Dreseris, Ema S., Ahmed, Sameen, Dupuis, Lucie, Stimec, Jennifer, Shago, Mary, Al-Hassnan, Zuhair N., Tremblay, Roch, Maass, Philipp G., Wilson, Michael D., Grunebaum, Eyal, Boycott, Kym M., Boisvert, François-Michel, Maddirevula, Sateesh, Faqeih, Eissa A., Almanjomi, Fahad, Khan, Zaheer Ullah, Alkuraya, Fowzan S., Campeau, Philippe M., Kannu, Peter, Campos, Eric I., Wurtele, Hugo

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Structural Variation of Chromosomes in Autism Spectrum Disorder por Marshall, Christian R., Noor, Abdul, Vincent, John B., Lionel, Anath C., Feuk, Lars, Skaug, Jennifer, Shago, Mary, Moessner, Rainald, Pinto, Dalila, Ren, Yan, Thiruvahindrapduram, Bhooma, Fiebig, Andreas, Schreiber, Stefan, Friedman, Jan, Ketelaars, Cees E.J., Vos, Yvonne J., Ficicioglu, Can, Kirkpatrick, Susan, Nicolson, Rob, Sloman, Leon, Summers, Anne, Gibbons, Clare A., Teebi, Ahmad, Chitayat, David, Weksberg, Rosanna, Thompson, Ann, Vardy, Cathy, Crosbie, Vicki, Luscombe, Sandra, Baatjes, Rebecca, Zwaigenbaum, Lonnie, Roberts, Wendy, Fernandez, Bridget, Szatmari, Peter, Scherer, Stephen W.

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BRAF Mutation and CDKN2A Deletion Define a Clinically Distinct Subgroup of Childhood Secondary High-Grade Glioma por Mistry, Matthew, Zhukova, Nataliya, Merico, Daniele, Rakopoulos, Patricia, Krishnatry, Rahul, Shago, Mary, Stavropoulos, James, Alon, Noa, Pole, Jason D., Ray, Peter N., Navickiene, Vilma, Mangerel, Joshua, Remke, Marc, Buczkowicz, Pawel, Ramaswamy, Vijay, Guerreiro Stucklin, Ana, Li, Martin, Young, Edwin J., Zhang, Cindy, Castelo-Branco, Pedro, Bakry, Doua, Laughlin, Suzanne, Shlien, Adam, Chan, Jennifer, Ligon, Keith L., Rutka, James T., Dirks, Peter B., Taylor, Michael D., Greenberg, Mark, Malkin, David, Huang, Annie, Bouffet, Eric, Hawkins, Cynthia E., Tabori, Uri

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The Diploid Genome Sequence of an Individual Human por Levy, Samuel, Sutton, Granger, Ng, Pauline C, Feuk, Lars, Halpern, Aaron L, Walenz, Brian P, Axelrod, Nelson, Huang, Jiaqi, Kirkness, Ewen F, Denisov, Gennady, Lin, Yuan, MacDonald, Jeffrey R, Pang, Andy Wing Chun, Shago, Mary, Stockwell, Timothy B, Tsiamouri, Alexia, Bafna, Vineet, Bansal, Vikas, Kravitz, Saul A, Busam, Dana A, Beeson, Karen Y, McIntosh, Tina C, Remington, Karin A, Abril, Josep F, Gill, John, Borman, Jon, Rogers, Yu-Hui, Frazier, Marvin E, Scherer, Stephen W, Strausberg, Robert L, Venter, J. Craig

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Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors por Anderson, Nathaniel D, de Borja, Richard, Young, Matthew D, Fuligni, Fabio, Rosic, Andrej, Roberts, Nicola D, Hajjar, Simon, Layeghifard, Mehdi, Novokmet, Ana, Kowalski, Paul E, Anaka, Matthew, Davidson, Scott, Zarrei, Mehdi, Said, Badr Id, Schreiner, L. Christine, Marchand, Remi, Sitter, Joseph, Gogkoz, Nalan, Brunga, Ledia, Graham, Garrett T, Fullam, Anthony, Pillay, Nischalan, Toretsky, Jeffrey A, Yoshida, Akihiko, Shibata, Tatsuhiro, Metzler, Markus, Somers, Gino R, Scherer, Stephen W, Flanagan, Adrienne M, Campbell, Peter J, Schiffman, Joshua D, Shago, Mary, Alexandrov, Ludmil B, Wunder, Jay S, Andrulis, Irene L, Malkin, David, Behjati, Sam, Shlien, Adam

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