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	1.	Isolated tetrasomy 13: a fifth case report of a rare chromosome abnormality associated with poorly differentiated acute myeloid leukemia. [electronic resource] by Roche-Lestienne, Catherine Richebourg, Steven Laï, Jean-Luc Andrieux, Joris Soenen-Cornu, Valérie Geffroy, Sandrine Producer: 20060818 In: Cancer genetics and cytogenetics vol. 168 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A novel type of [electronic resource] by Duployez, Nicolas Chebrek, Lydia Helevaut, Nathalie Fournier, Elise Bemba, Maxime Caillault, Aurélie Geffroy, Sandrine Preudhomme, Claude Producer: 20191021 In: Haematologica vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Cryptic 6p21.3 duplications and triplication involving HMGA1 partially masked by add 6p in four cases of myelodysplasia. [electronic resource] by Andrieux, Joris Geffroy, Sandrine Bilhou-Nabera, Chrystèle Dupriez, Brigitte Demory, Jean Loup Bauters, Francis Laï, Jean Luc Dastugue, Nicole Producer: 20060209 In: Cancer genetics and cytogenetics vol. 164 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Familial occurrence of thymoma and autoimmune diseases with the constitutional translocation t(14;20)(q24.1;p12.3). [electronic resource] by Nicodème, Frédéric Geffroy, Sandrine Conti, Massimo Delobel, Bruno Soenen, Valérie Grardel, Nathalie Porte, Henri Copin, Marie-Christine Laï, Jean-Luc Andrieux, Joris Producer: 20050926 In: Genes, chromosomes & cancer vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	RUNX1 DNA-binding mutations and RUNX1-PRDM16 cryptic fusions in BCR-ABL+ leukemias are frequently associated with secondary trisomy 21 and may contribute to clonal evolution and imatinib resistance. [electronic resource] by Roche-Lestienne, Catherine Deluche, Lauréline Corm, Sélim Tigaud, Isabelle Joha, Sami Philippe, Nathalie Geffroy, Sandrine Laï, Jean-Luc Nicolini, Franck-Emmanuel Preudhomme, Claude Producer: 20080515 In: Blood vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Cryptic and partial deletions of PRDM16 and RUNX1 without t(1;21)(p36;q22) and/or RUNX1-PRDM16 fusion in a case of progressive chronic myeloid leukemia: a complex chromosomal rearrangement of underestimated frequency in disease progression? [electronic resource] by Deluche, Lauréline Joha, Sami Corm, Sélim Daudignon, Agnès Geffroy, Sandrine Quief, Sabine Villenet, Céline Kerckaert, Jean-Pierre Laï, Jean-Luc Preudhomme, Claude Roche-Lestienne, Catherine Producer: 20081208 In: Genes, chromosomes & cancer vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Detection of a new heterozygous germline ETV6 mutation in a case with hyperdiploid acute lymphoblastic leukemia. [electronic resource] by Duployez, Nicolas Abou Chahla, Wadih Lejeune, Sophie Marceau-Renaut, Alice Letizia, Guillaume Boyer, Thomas Geffroy, Sandrine Peyrouze, Pauline Grardel, Nathalie Nelken, Brigitte Michel, Gérard Bertrand, Yves Preudhomme, Claude Producer: 20180723 In: European journal of haematology vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Bone morphogenetic protein antagonist gene NOG is involved in myeloproliferative disease associated with myelofibrosis. [electronic resource] by Andrieux, Joris Roche-Lestienne, Catherine Geffroy, Sandrine Desterke, Christophe Grardel, Nathalie Plantier, Isabelle Selleslag, Dominik Demory, Jean-Loup Laï, Jean-Luc Leleu, Xavier Le Bousse-Kerdiles, Caroline Vandenberghe, Peter Producer: 20071109 In: Cancer genetics and cytogenetics vol. 178 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Unlike ASXL1 and ASXL2 mutations, ASXL3 mutations are rare events in acute myeloid leukemia with t(8;21). [electronic resource] by Duployez, Nicolas Micol, Jean-Baptiste Boissel, Nicolas Petit, Arnaud Geffroy, Sandrine Bucci, Maxime Lapillonne, Hélène Renneville, Aline Leverger, Guy Ifrah, Norbert Dombret, Hervé Abdel-Wahab, Omar Jourdan, Eric Preudhomme, Claude Producer: 20161013 In: Leukemia & lymphoma vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Clinical relevance of [electronic resource] by Ferret, Yann Boissel, Nicolas Helevaut, Nathalie Madic, Jordan Nibourel, Olivier Marceau-Renaut, Alice Bucci, Maxime Geffroy, Sandrine Celli-Lebras, Karine Castaigne, Sylvie Thomas, Xavier Terré, Christine Dombret, Hervé Preudhomme, Claude Renneville, Aline Producer: 20190708 In: Haematologica vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Prognostic impact of isocitrate dehydrogenase enzyme isoforms 1 and 2 mutations in acute myeloid leukemia: a study by the Acute Leukemia French Association group. [electronic resource] by Boissel, Nicolas Nibourel, Olivier Renneville, Aline Gardin, Claude Reman, Oumedaly Contentin, Nathalie Bordessoule, Dominique Pautas, Cécile de Revel, Thierry Quesnel, Bruno Huchette, Pascal Philippe, Nathalie Geffroy, Sandrine Terre, Christine Thomas, Xavier Castaigne, Sylvie Dombret, Hervé Preudhomme, Claude Producer: 20100928 In: Journal of clinical oncology : official journal of the American Society of Clinical Oncology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Frequent ASXL2 mutations in acute myeloid leukemia patients with t(8;21)/RUNX1-RUNX1T1 chromosomal translocations. [electronic resource] by Micol, Jean-Baptiste Duployez, Nicolas Boissel, Nicolas Petit, Arnaud Geffroy, Sandrine Nibourel, Olivier Lacombe, Catherine Lapillonne, Helene Etancelin, Pascaline Figeac, Martin Renneville, Aline Castaigne, Sylvie Leverger, Guy Ifrah, Norbert Dombret, Hervé Preudhomme, Claude Abdel-Wahab, Omar Jourdan, Eric Producer: 20150424 In: Blood vol. 124 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome. [electronic resource] by Poulain, Stéphanie Boyle, Eileen M Roumier, Christophe Demarquette, Hélène Wemeau, Mathieu Geffroy, Sandrine Herbaux, Charles Bertrand, Elisabeth Hivert, Bénédicte Terriou, Louis Verrier, Albert Pollet, Jean Paul Maurage, Claude Alain Onraed, Brigitte Morschhauser, Franck Quesnel, Bruno Duthilleul, Patrick Preudhomme, Claude Leleu, Xavier Producer: 20150311 In: British journal of haematology vol. 167 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	None [electronic resource] by Poulain, Stéphanie Roumier, Christophe Bertrand, Elisabeth Renneville, Aline Caillault-Venet, Aurélie Doye, Emmanuelle Geffroy, Sandrine Sebda, Sheherazade Nibourel, Olivier Nudel, Morgane Herbaux, Charles Renaud, Loic Tomowiak, Cécile Guidez, Stéphanie Tricot, Sabine Roche-Lestienne, Catherine Quesnel, Bruno Preudhomme, Claude Leleu, Xavier Producer: 20180523 In: Clinical cancer research : an official journal of the American Association for Cancer Research vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Incidence and prognostic value of TET2 alterations in de novo acute myeloid leukemia achieving complete remission. [electronic resource] by Nibourel, Olivier Kosmider, Olivier Cheok, Meyling Boissel, Nicolas Renneville, Aline Philippe, Nathalie Dombret, Hervé Dreyfus, François Quesnel, Bruno Geffroy, Sandrine Quentin, Samuel Roche-Lestienne, Catherine Cayuela, Jean-Michel Roumier, Christophe Fenaux, Pierre Vainchenker, William Bernard, Olivier A Soulier, Jean Fontenay, Michaëla Preudhomme, Claude Producer: 20100928 In: Blood vol. 116 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	SNP-array lesions in core binding factor acute myeloid leukemia. [electronic resource] by Duployez, Nicolas Boudry-Labis, Elise Roumier, Christophe Boissel, Nicolas Petit, Arnaud Geffroy, Sandrine Helevaut, Nathalie Celli-Lebras, Karine Terré, Christine Fenneteau, Odile Cuccuini, Wendy Luquet, Isabelle Lapillonne, Hélène Lacombe, Catherine Cornillet, Pascale Ifrah, Norbert Dombret, Hervé Leverger, Guy Jourdan, Eric Preudhomme, Claude Publication details: Oncotarget Jan 2018 In: Oncotarget vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Clofarabine Improves Relapse-Free Survival of Acute Myeloid Leukemia in Younger Adults with Micro-Complex Karyotype. [electronic resource] by Fenwarth, Laurène Duployez, Nicolas Thomas, Xavier Boissel, Nicolas Geffroy, Sandrine Marceau-Renaut, Alice Caillot, Denis Raffoux, Emmanuel Lemasle, Emilie Marolleau, Jean-Pierre Berthon, Céline Cheok, Meyling H Peyrouze, Pauline Pigneux, Arnaud Vey, Norbert Celli-Lebras, Karine Terré, Christine Preudhomme, Claude Dombret, Hervé Publication details: Cancers Dec 2019 In: Cancers vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Molecular Profiling Defines Distinct Prognostic Subgroups in Childhood AML: A Report From the French ELAM02 Study Group. [electronic resource] by Marceau-Renaut, Alice Duployez, Nicolas Ducourneau, Benoît Labopin, Myriam Petit, Arnaud Rousseau, Alexandra Geffroy, Sandrine Bucci, Maxime Cuccuini, Wendy Fenneteau, Odile Ruminy, Philippe Nelken, Brigitte Ducassou, Stéphane Gandemer, Virginie Leblanc, Thierry Michel, Gérard Bertrand, Yves Baruchel, André Leverger, Guy Preudhomme, Claude Lapillonne, Hélène Publication details: HemaSphere In: HemaSphere vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Genomic Landscape of CXCR4 Mutations in Waldenström Macroglobulinemia. [electronic resource] by Poulain, Stéphanie Roumier, Christophe Venet-Caillault, Aurélie Figeac, Martin Herbaux, Charles Marot, Guillemette Doye, Emmanuelle Bertrand, Elisabeth Geffroy, Sandrine Lepretre, Frédéric Nibourel, Olivier Decambron, Audrey Boyle, Eileen Mary Renneville, Aline Tricot, Sabine Daudignon, Agnès Quesnel, Bruno Duthilleul, Patrick Preudhomme, Claude Leleu, Xavier Producer: 20161213 In: Clinical cancer research : an official journal of the American Association for Cancer Research vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Neurofibromatosis-1 gene deletions and mutations in de novo adult acute myeloid leukemia. [electronic resource] by Boudry-Labis, Elise Roche-Lestienne, Catherine Nibourel, Olivier Boissel, Nicolas Terre, Christine Perot, Christine Eclache, Virginie Gachard, Nathalie Tigaud, Isabelle Plessis, Ghislaine Cuccuini, Wendy Geffroy, Sandrine Villenet, Céline Figeac, Martin Leprêtre, Frederic Renneville, Aline Cheok, Meyling Soulier, Jean Dombret, Hervé Preudhomme, Claude Producer: 20130510 In: American journal of hematology vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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