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There are 6289 results for: content related to: DNA sequencing of maternal plasma to identify Down syndrome and other trisomies in multiple gestations

  1. A study of reciprocal translocations and inversions detected by light microscopy with special reference to origin, segregation, and recurrent abnormalities

    American Journal of Medical Genetics Part A

    Volume 126A, Issue 1, 1 April 2004, Pages: 46–60, Sheila Youings, Katrina Ellis, Sarah Ennis, John Barber and Patricia Jacobs

    Version of Record online : 23 DEC 2003, DOI: 10.1002/ajmg.a.20553

  2. Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci

    Prenatal Diagnosis

    Volume 32, Issue 13, December 2012, Pages: 1233–1241, Bernhard Zimmermann, Matthew Hill, George Gemelos, Zachary Demko, Milena Banjevic, Johan Baner, Allison Ryan, Styrmir Sigurjonsson, Nikhil Chopra, Michael Dodd, Brynn Levy and Matthew Rabinowitz

    Version of Record online : 30 OCT 2012, DOI: 10.1002/pd.3993

  3. Sex-specific chromosome instability in early human development

    American Journal of Medical Genetics Part A

    Volume 136A, Issue 4, 1 August 2005, Pages: 401–413, Natalia V. Kovaleva

    Version of Record online : 6 JUL 2005, DOI: 10.1002/ajmg.a.30815

  4. Cytogenetic analysis of 101 giant cell tumors of bone: Nonrandom patterns of telomeric associations and other structural aberrations

    Genes, Chromosomes and Cancer

    Volume 48, Issue 7, July 2009, Pages: 583–602, Ludmila Gorunova, Fredrik Vult von Steyern, Clelia Tiziana Storlazzi, Bodil Bjerkehagen, Gunnar Follerås, Sverre Heim, Nils Mandahl and Fredrik Mertens

    Version of Record online : 24 APR 2009, DOI: 10.1002/gcc.20667

  5. Population-based study of cancer among carriers of a constitutional structural chromosomal rearrangement

    Genes, Chromosomes and Cancer

    Volume 45, Issue 3, March 2006, Pages: 231–246, Iben Bache, Henrik Hasle, Niels Tommerup and Jørgen H. Olsen

    Version of Record online : 9 NOV 2005, DOI: 10.1002/gcc.20285

  6. Incidence and prognostic impact of secondary cytogenetic aberrations in a series of 145 patients with mantle cell lymphoma

    Genes, Chromosomes and Cancer

    Volume 49, Issue 5, May 2010, Pages: 439–451, Blanca Espinet, Itziar Salaverria, Sílvia Beà, Neus Ruiz-Xivillé, Olga Balagué, Marta Salido, Dolors Costa, Joaquim Carreras, Ana Eugenia Rodríguez-Vicente, Juan Luís García, Jesús María Hernández-Rivas, María José Calasanz, Reiner Siebert, Ana Ferrer, Antonio Salar, Ana Carrió, Natividad Polo, José Antonio García-Marco, Alicia Domingo, Eva González-Barca, Vicenç Romagosa, Isabel Marugán, Armando López-Guillermo, Fuensanta Millá, José Luís Mate, Elisa Luño, Carmen Sanzo, Rosa Collado, Isabel Oliver, Sebastià Monzó, Antonio Palacín, Teresa González, Francesc Sant, Ramon Salinas, María Teresa Ardanaz, Llorenç Font, Lourdes Escoda, Lourdes Florensa, Sergi Serrano, Elias Campo and Francesc Solé

    Version of Record online : 8 FEB 2010, DOI: 10.1002/gcc.20754

  7. Cytogenetic features of multiple myeloma: impact of gender, age, disease phase, culture time, and cytokine stimulation

    European Journal of Haematology

    Volume 68, Issue 6, June 2002, Pages: 345–353, T. Nilsson, S. Lenhoff, I. Turesson, L. Rylander, F. Mitelman, J. Westin, M. Höglund and B. Johansson

    Version of Record online : 13 SEP 2002, DOI: 10.1034/j.1600-0609.2002.00724.x

  8. New recurrent balanced translocations in acute myeloid leukemia and myelodysplastic syndromes: Cancer and leukemia group B 8461

    Genes, Chromosomes and Cancer

    Volume 52, Issue 4, April 2013, Pages: 385–401, Alison Walker, Krzysztof Mrózek, Jessica Kohlschmidt, Kathleen W. Rao, Mark J. Pettenati, Lisa J. Sterling, Guido Marcucci, Andrew J. Carroll, Clara D. Bloomfield and for the Alliance for Clinical Trials in Oncology

    Version of Record online : 10 DEC 2012, DOI: 10.1002/gcc.22036

  9. You have free access to this content
    Poster Abstracts of the ISPD 21st International Conference on Prenatal Diagnosis and Therapy, San Diego, California, USA, 9-12 July 2017

    Prenatal Diagnosis

    Volume 37, Issue S1, July 2017, Pages: 21–105,

    Version of Record online : 5 JUL 2017, DOI: 10.1002/pd.5085

  10. Reevaluating confined placental mosaicism

    American Journal of Medical Genetics Part A

    Volume 131A, Issue 3, 15 December 2004, Pages: 232–239, Gail Stetten, Cathleen S. Escallon, Sarah T. South, Joseph L. McMichael, Daniel O. Saul and Karin J. Blakemore

    Version of Record online : 4 NOV 2004, DOI: 10.1002/ajmg.a.30363

  11. Cytogenetic manifestations of multiple myeloma heterogeneity

    Genes, Chromosomes and Cancer

    Volume 42, Issue 1, January 2005, Pages: 44–57, Dimitra Pantou, Helen Rizou, Haroula Tsarouha, Anastasia Pouli, Kostas Papanastasiou, Marina Stamatellou, Theoni Trangas, Nikos Pandis and Georgia Bardi

    Version of Record online : 19 OCT 2004, DOI: 10.1002/gcc.20114

  12. Reassessment of childhood B-lineage lymphoblastic leukemia karyotypes using spectral analysis

    Genes, Chromosomes and Cancer

    Volume 30, Issue 4, April 2001, Pages: 383–392, Hatem Elghezal, Gaëlle Le Guyader, Isabella Radford-Weiss, Christine Perot, Jacqueline Van Den Akker, Patrice Eydoux, Michel Vekemans and Serge P. Romana

    Version of Record online : 1 MAR 2001, DOI: 10.1002/gcc.1104

  13. You have free access to this content
    The prognosis for patients with chronic myeloid leukemia who have clonal cytogenetic abnormalities in philadelphia chromosome-negative cells


    Volume 110, Issue 7, 1 October 2007, Pages: 1509–1519, Michael W. N. Deininger, Jorge Cortes, Ron Paquette, Byung Park, Andreas Hochhaus, Michele Baccarani, Richard Stone, Thomas Fischer, Hagop Kantarjian, Dietger Niederwieser, Carlo Gambacorti-Passerini, Charlene So, Insa Gathmann, John M. Goldman, Douglas Smith, Brian J. Druker and François Guilhot

    Version of Record online : 14 AUG 2007, DOI: 10.1002/cncr.22936

  14. Prospective study of 174 de novo acute myelogenous leukemias according to the WHO classification: subtypes, cytogenetic features and FLT3 mutations

    European Journal of Haematology

    Volume 77, Issue 1, July 2006, Pages: 35–45, Liming Bao, Xiaoqin Wang, John Ryder, Meirong Ji, Yan Chen, Hui Chen, Hengjuan Sun, Yongchen Yang, Xinyu Du, Patrick Kerzic, Sherilyn A. Gross, Lihong Yao, Ling Lv, Hua Fu, Guowei Lin and Richard D. Irons

    Version of Record online : 27 MAR 2006, DOI: 10.1111/j.1600-0609.2006.00660.x

  15. Cytogenetic abnormalities in essential thrombocythemia: prevalence and prognostic significance

    European Journal of Haematology

    Volume 83, Issue 1, July 2009, Pages: 17–21, Naseema Gangat, Ayalew Tefferi, Gita Thanarajasingam, Mrinal Patnaik, Susan Schwager, Rhett Ketterling and Alexandra P. Wolanskyj

    Version of Record online : 19 FEB 2009, DOI: 10.1111/j.1600-0609.2009.01246.x

  16. You have free access to this content
    Stability of leukemia-associated aberrant immunophenotypes in patients with acute myeloid leukemia between diagnosis and relapse: Comparison with cytomorphologic, cytogenetic, and molecular genetic findings

    Cytometry Part B: Clinical Cytometry

    Volume 62B, Issue 1, November 2004, Pages: 25–38, Daniela Voskova, Claudia Schoch, Susanne Schnittger, Wolfgang Hiddemann, Torsten Haferlach and Wolfgang Kern

    Version of Record online : 4 OCT 2004, DOI: 10.1002/cyto.b.20025

  17. Genomic array as compared to karyotyping in myelodysplastic syndromes in a prospective clinical trial

    Genes, Chromosomes and Cancer

    Volume 56, Issue 7, July 2017, Pages: 524–534, Marian J. Stevens-Kroef, Daniel Olde Weghuis, Najat ElIdrissi-Zaynoun, Bert van der Reijden, Eline M. P. Cremers, Canan Alhan, Theresia M. Westers, Heleen A. Visser-Wisselaar, Dana A. Chitu, Sonia M. Cunha, Edo Vellenga, Saskia K. Klein, Pierre Wijermans, Georgine E. de Greef, M. Ron Schaafsma, Petra Muus, Gert J. Ossenkoppele, Arjan A. van de Loosdrecht and Joop H. Jansen

    Version of Record online : 31 MAR 2017, DOI: 10.1002/gcc.22455

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    Karyotypic characterization of papillary thyroid carcinomas


    Volume 92, Issue 10, 15 November 2001, Pages: 2529–2538, Lucia Roque, Vasco M. Nunes, Catarina Ribeiro, Carmo Martins and Jorge Soares

    Version of Record online : 31 OCT 2001, DOI: 10.1002/1097-0142(20011115)92:10<2529::AID-CNCR1604>3.0.CO;2-M

  19. Novel recurrent chromosome anomalies in Shwachman–Diamond syndrome

    Pediatric Blood & Cancer

    Volume 64, Issue 8, August 2017, Roberto Valli, Elena De Paoli, Lucia Nacci, Annalisa Frattini, Francesco Pasquali and Emanuela Maserati

    Version of Record online : 28 JAN 2017, DOI: 10.1002/pbc.26454

  20. Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies

    Genes, Chromosomes and Cancer

    Volume 45, Issue 4, April 2006, Pages: 375–382, Emanuela Maserati, Antonella Minelli, Barbara Pressato, Roberto Valli, Barbara Crescenzi, Maurizio Stefanelli, Giuseppe Menna, Laura Sainati, Furio Poli, Claudio Panarello, Marco Zecca, Francesco Lo Curto, Cristina Mecucci, Cesare Danesino and Francesco Pasquali

    Version of Record online : 28 DEC 2005, DOI: 10.1002/gcc.20301