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There are 5426 results for: content related to: Inheritance of the chronic myeloproliferative neoplasms. A systematic review

  1. You have free access to this content
    JAK2 and genomic instability in the myeloproliferative neoplasms: A case of the chicken or the egg?

    American Journal of Hematology

    Volume 87, Issue 11, November 2012, Pages: 1028–1036, Linda M. Scott and Vivienne I. Rebel

    Article first published online : 28 MAY 2012, DOI: 10.1002/ajh.23243

  2. Mutation analysis of ASXL1, CBL, DNMT3A, IDH1, IDH2, JAK2, MPL, NF1, SF3B1, SUZ12, and TET2 in myeloproliferative neoplasms

    Genes, Chromosomes and Cancer

    Volume 51, Issue 8, August 2012, Pages: 743–755, Mandy Brecqueville, Jérôme Rey, François Bertucci, Emilie Coppin, Pascal Finetti, Nadine Carbuccia, Nathalie Cervera, Véronique Gelsi-Boyer, Christine Arnoulet, Olivier Gisserot, Denis Verrot, Borhane Slama, Norbert Vey, Marie-Joelle Mozziconacci, Daniel Birnbaum and Anne Murati

    Article first published online : 9 APR 2012, DOI: 10.1002/gcc.21960

  3. You have free access to this content
    Unraveling the genetic underpinnings of myeloproliferative neoplasms and understanding their effect on disease course and response to therapy: Proceedings from the 6th international post-ASH symposium

    American Journal of Hematology

    Volume 87, Issue 5, May 2012, Pages: 562–568, Omar Abdel-Wahab, Animesh Pardanani, Olivier A. Bernard, Guido Finazzi, John D. Crispino, Heinz Gisslinger, Robert Kralovics, Olatoyosi Odenike, Kapil Bhalla, Vikas Gupta, Giovanni Barosi, Jason Gotlib, Paola Guglielmelli, Jean-Jacques Kiladjian, Pierre Noel, Mario Cazzola, Alessandro M. Vannucchi, Ronald Hoffman, Tiziano Barbui, Juergen Thiele, Richard A. Van Etten, Tariq Mughal and Ayalew Tefferi

    Article first published online : 28 MAR 2012, DOI: 10.1002/ajh.23169

  4. Myeloproliferative Neoplasms: New Translational Therapies

    Mount Sinai Journal of Medicine: A Journal of Translational and Personalized Medicine

    Volume 77, Issue 6, November/December 2010, Pages: 667–683, John Mascarenhas and Ronald Hoffman

    Article first published online : 23 NOV 2010, DOI: 10.1002/msj.20225

  5. The early-life social environment and DNA methylation

    Clinical Genetics

    Volume 81, Issue 4, April 2012, Pages: 341–349, M Szyf

    Article first published online : 13 FEB 2012, DOI: 10.1111/j.1399-0004.2012.01843.x

  6. Hematopoietic clonal dominance, stem cell mutations, and evolutionary pattern of JAK2V617F allele burden in polycythemia vera

    European Journal of Haematology

    Volume 94, Issue 3, March 2015, Pages: 251–257, Anna Angona, Alberto Alvarez-Larrán, Beatriz Bellosillo, Luz Martínez-Avilés, Laura Camacho, Concepción Fernández-Rodríguez, Silvia Pairet, Raquel Longarón, Águeda Ancochea, Alicia Senín, Lourdes Florensa and Carles Besses

    Article first published online : 13 SEP 2014, DOI: 10.1111/ejh.12425

  7. You have full text access to this Open Access content
    Epigenetic therapy in myeloproliferative neoplasms: evidence and perspectives

    Journal of Cellular and Molecular Medicine

    Volume 13, Issue 8a, August 2009, Pages: 1437–1450, Alessandro M. Vannucchi, Paola Guglielmelli, Alessandro Rambaldi, Costanza Bogani and Tiziano Barbui

    Article first published online : 11 JUN 2009, DOI: 10.1111/j.1582-4934.2009.00827.x

  8. Myeloproliferative Neoplasms: Chronic Myelogenous Leukemia, Polycythemia Vera, Essential Thrombocythemia, and Primary Myelofibrosis

    Textbook of Uncommon Cancer

    Raoul Tibes, Gurcharan Singh Khera, Ruben A. Mesa, Pages: 647–658, 2012

    Published Online : 20 SEP 2012, DOI: 10.1002/9781118464557.ch47

  9. History of genetics through philately – deafness

    Clinical Genetics

    Volume 60, Issue 6, December 2001, Pages: 417–420, SM Nikkel and AE Chudley

    Article first published online : 11 JAN 2002, DOI: 10.1034/j.1399-0004.2001.600603.x

  10. Landmarks in genetics through philately: the tools used by dysmorphologists

    Clinical Genetics

    Volume 63, Issue 2, February 2003, Pages: 105–108, AE Chudley

    Article first published online : 10 MAR 2003, DOI: 10.1034/j.1399-0004.2003.00030.x

  11. Retinal detachment and cataract, facial dysmorphism, generalized osteoporosis, immobile spine and platyspondyly in a consanguinous kindred – a possible new syndrome

    Clinical Genetics

    Volume 59, Issue 2, February 2001, Pages: 99–105, H Schmidt, G Rudolph, M Hergersberg, K Schneider, S Moradi and T Meitinger*

    Article first published online : 20 DEC 2001, DOI: 10.1034/j.1399-0004.2001.590206.x

  12. Interpupillary distance in a normal black population

    Clinical Genetics

    Volume 55, Issue 3, March 1999, Pages: 182–191, EK Pivnick, ML Rivas, EA Tolley, SD Smith and GJ Presbury

    Article first published online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.1999.550306.x

  13. Partial DiGeorge syndrome in two patients with a 10p rearrangement

    Clinical Genetics

    Volume 55, Issue 4, April 1999, Pages: 269–276, Hilde Van Esch, Peter Groenen, Sarah Daw, Ann Poffyn, Maureen Holvoet, Peter Scambler, Jean-Pierre Fryns, Wim Van de Ven and Koen Devriendt

    Article first published online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.1999.550410.x

  14. A new classification system for primary lymphatic dysplasias based on phenotype

    Clinical Genetics

    Volume 77, Issue 5, May 2010, Pages: 438–452, F Connell, G Brice, S Jeffery, V Keeley, P Mortimer and S Mansour

    Article first published online : 11 FEB 2010, DOI: 10.1111/j.1399-0004.2010.01394.x

  15. You have free access to this content
    The JAK2 exon 12 mutations: A comprehensive review

    American Journal of Hematology

    Volume 86, Issue 8, August 2011, Pages: 668–676, Linda M. Scott

    Article first published online : 14 JUN 2011, DOI: 10.1002/ajh.22063

  16. 40 years of the annual ‘Bar Harbor Course’ (1960–1999): a pictorial history

    Clinical Genetics

    Volume 55, Issue 6, June 1999, Pages: 398–415, Victor A McKusick, Juergen Naggert, Patsy Nishina and David Valle

    Article first published online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.1999.550603.x

  17. Neurodevelopmental consequences of maternal distress: what do we really know?

    Clinical Genetics

    Volume 83, Issue 2, February 2013, Pages: 108–117, C Schuurmans and DM Kurrasch

    Article first published online : 6 DEC 2012, DOI: 10.1111/cge.12049

  18. You have free access to this content
    Prevalence and clinical outcomes of the 46/1 haplotype, Janus kinase 2 mutations, and ten-eleven translocation 2 mutations in budd-chiari syndrome and their impact on thrombotic complications post Liver Transplantation

    Liver Transplantation

    Volume 18, Issue 7, July 2012, Pages: 819–827, Rachel H. Westbrook, Nicholas C. Lea, Azim M. Mohamedali, Alexander E. Smith, David W. Orr, Lara N. Roberts, Nigel D. Heaton, Julia A. Wendon, John G. O'Grady, Michael A. Heneghan and Ghulam J. Mufti

    Article first published online : 12 JUL 2012, DOI: 10.1002/lt.23443

  19. Chimera and other fertilization errors

    Clinical Genetics

    Volume 70, Issue 5, November 2006, Pages: 363–373, V Malan, M Vekemans and C Turleau

    Article first published online : 14 SEP 2006, DOI: 10.1111/j.1399-0004.2006.00689.x

  20. Identification of four novel mutations in five unrelated Korean families with Fabry disease

    Clinical Genetics

    Volume 58, Issue 3, September 2000, Pages: 228–233, J-K Lee, G-H Kim, J-S Kim, K-K Kim, M-C Lee and H-W Yoo

    Article first published online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.2000.580311.x