Resultados de búsqueda - Harriet Druker

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  1. 1
    Younger Age of Cancer Initiation Is Associated with Shorter Telomere Length in Li-Fraumeni Syndrome

    Younger Age of Cancer Initiation Is Associated with Shorter Telomere Length in Li-Fraumeni Syndrome por Uri Tabori, Sonia Nanda, Harriet Druker, Jodi Lees, David Malkin

    Publicado 2007
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  2. 2
    Cancer and Central Nervous System Tumor Surveillance in Pediatric Neurofibromatosis 2 and Related Disorders

    Cancer and Central Nervous System Tumor Surveillance in Pediatric Neurofibromatosis 2 and Related Disorders por D. Gareth Evans, Héctor Salvador, Vivian Y. Chang, Ayelet Erez, Stephan D. Voss, Harriet Druker, Hamish S. Scott, Uri Tabori

    Publicado 2017
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  3. 3
    Excessive genomic DNA copy number variation in the Li–Fraumeni cancer predisposition syndrome

    Excessive genomic DNA copy number variation in the Li–Fraumeni cancer predisposition syndrome por Adam Shlien, Uri Tabori, Christian R. Marshall, Małgorzata Pieńkowska, Lars Feuk, Ana Novokmet, Sonia Nanda, Harriet Druker, Stephen W. Scherer, David Malkin

    Publicado 2008
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  4. 4
    Von Hippel–Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood

    Von Hippel–Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood por Surya P. Rednam, Ayelet Erez, Harriet Druker, Katherine A. Janeway, Junne Kamihara, Wendy Kohlmann, Katherine L. Nathanson, Lisa J. States, Gail E. Tomlinson, Anita Villani, Stephan D. Voss, Joshua D. Schiffman, Jonathan D. Wasserman

    Publicado 2017
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  5. 5
    A Common Molecular Mechanism Underlies Two Phenotypically Distinct 17p13.1 Microdeletion Syndromes

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

    Publicado 2010
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  6. 6
    Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood

    Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood por Jonathan D. Wasserman, Gail E. Tomlinson, Harriet Druker, Junne Kamihara, Wendy Kohlmann, Christian P. Kratz, Katherine L. Nathanson, Kristian W. Pajtler, Andreu Parareda, Surya P. Rednam, Lisa J. States, Anita Villani, Michael F. Walsh, Kristin Zelley, Joshua D. Schiffman

    Publicado 2017
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  7. 7
    Cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal Cancer Syndromes in Childhood

    Cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal Cancer Syndromes in Childhood por Maria Isabel Achatz, Christopher C. Porter, Laurence Brugières, Harriet Druker, Thierry Frébourg, William D. Foulkes, Christian P. Kratz, Roland P. Kuiper, Jordan R. Hansford, Héctor Salvador, Katherine L. Nathanson, Wendy Kohlmann, Leslie Doros, Kenan Onel, Kami Wolfe Schneider, Sarah Scollon, Uri Tabori, Gail E. Tomlinson, D. Gareth Evans, Sharon E. Plon

    Publicado 2017
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  8. 8
    Germ-line and somatic DICER1 mutations in pineoblastoma

    Germ-line and somatic DICER1 mutations in pineoblastoma por Leanne de Kock, Nelly Sabbaghian, Harriet Druker, Evan Weber, Nancy Hamel, S. Miller, Catherine S Choong, Nicholas G. Gottardo, Ursula R. Kees, Surya P. Rednam, Liselotte P. van Hest, Marjolijn C.J. Jongmans, Shalini N. Jhangiani, James R. Lupski, Margaret Zacharin, Dorothée Bouron‐Dal Soglio, Annie Huang, John R. Priest, Arie Perry, Sabine Mueller, Steffen Albrecht, David Malkin, Richard G. Grundy, William D. Foulkes

    Publicado 2014
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  9. 9
    Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors

    Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors por Jonathon Torchia, Brian Golbourn, Shengrui Feng, King Ching Ho, Patrick Sin‐Chan, Alexandre Vasiljevic, Joseph Norman, Paul Guilhamon, Livia Garzia, Natalia R. Agamez, Mei Lu, Tiffany Sin Yu Chan, Daniel Picard, Pasqualino de Antonellis, Dong-Anh Khuong-Quang, Aline Cristiane Planello, Constanze Zeller, Dalia Baršytė-Lovejoy, Lucie Lafay‐Cousin, Louis Létourneau, Mathieu Bourgey, Man Yu, Deena M.A. Gendoo, Misko Dzamba, Mark Barszczyk, Tiago da Silva Medina, Alexandra N. Riemenschneider, A. Sorana Morrissy, Young‐Shin Ra, Vijay Ramaswamy, Marc Remke, Christopher Dunham, Stephen Yip, Ho‐Keung Ng, Jian‐Qiang Lu, Vivek Mehta, Steffen Albrecht, José Pimentel, Jennifer A. Chan, Gino R. Somers, Cláudia C. Faria, Lúcia Roque, Maryam Fouladi, Lindsey M. Hoffman, Andrew S. Moore, Yin Wang, Seung Ah Choi, Jordan R. Hansford, Daniel Catchpoole, Diane K. Birks, Nicholas K. Foreman, Doug Strother, Álmos Klekner, László Bognár, Miklós Garami, Péter Hauser, Tibor Hortobágyi, Beverly Wilson, Juliette Hukin, Anne-Sophie Carret, Timothy Van Meter, Eugene Hwang, Amar Gajjar, Shih‐Hwa Chiou, Hideo Nakamura, Helen Toledano, Iris Fried, Daniel W. Fults, Takafumi Wataya, Chris Fryer, David D. Eisenstat, Katrin Scheinemann, Adam Fleming, Donna L. Johnston, Jean Michaud, Shayna Zelcer, Robert Hammond, Samina Afzal, David A. Ramsay, Nongnuch Sirachainan, Suradej Hongeng, Noppadol Larbcharoensub, Richard G. Grundy, Rishi Lulla, Jason Fangusaro, Harriet Druker, Ute Bartels, Ronald Grant, David Malkin, C. Jane McGlade, Theodore Nicolaides, Tarık Tihan, Joanna J. Phillips, Jacek Majewski, Alexandre Montpetit, Guillaume Bourque, Gary D. Bader, Alyssa Reddy, G. Yancey Gillespie, Monika Warmuth‐Metz

    Publicado 2016
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