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There are 30858 results for: content related to: A boy with partial trisomy of chromosome 3q24–q28 from paternal balanced insertion and multiple congenital anomalies

  1. Omphalocele in trisomy 3q: further delineation of phenotype

    Clinical Genetics

    Volume 64, Issue 5, November 2003, Pages: 404–413, SA Yatsenko, R Mendoza-Londono, JW Belmont and LG Shaffer

    Article first published online : 21 OCT 2003, DOI: 10.1034/j.1399-0004.2003.00159.x

  2. Novel case of dup(3q) syndrome due to a de novo interstitial duplication 3q24-q26.31 with minimal overlap to the dup(3q) critical region

    American Journal of Medical Genetics Part A

    Volume 132A, Issue 1, 1 January 2005, Pages: 84–89, Moritz Meins, Javad Karimzad Hagh, Fritz Gerresheim, Elisabeth Einhoff, Heidi Olschewski, Henning Strehl and Jörg T. Epplen

    Article first published online : 18 NOV 2004, DOI: 10.1002/ajmg.a.30384

  3. Complex chromosomal rearrangements leading to MECOM overexpression are recurrent in myeloid malignancies with various 3q abnormalities

    Genes, Chromosomes and Cancer

    Volume 55, Issue 4, April 2016, Pages: 375–388, Carmen Baldazzi, Simona Luatti, Elisa Zuffa, Cristina Papayannidis, Emanuela Ottaviani, Giulia Marzocchi, Gaia Ameli, Maria Antonella Bardi, Laura Bonaldi, Rossella Paolini, Carmela Gurrieri, Gian Matteo Rigolin, Antonio Cuneo, Giovanni Martinelli, Michele Cavo and Nicoletta Testoni

    Article first published online : 27 JAN 2016, DOI: 10.1002/gcc.22341

  4. A girl with inverted triplication of chromosome 3q25.3 [RIGHTWARDS ARROW] q29 and multiple congenital anomalies consistent with 3q duplication syndrome

    American Journal of Medical Genetics Part A

    Volume 134A, Issue 4, 1 May 2005, Pages: 434–438, Katrin Õunap, Tiiu Ilus and Oliver Bartsch

    Article first published online : 25 MAR 2005, DOI: 10.1002/ajmg.a.30134

  5. Neocentromere marker chromosome of distal 3q mimicking dup(3q) syndrome phenotype

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 15, 1 August 2008, Pages: 1967–1971, Kosuke Izumi, Yukio Yamashita, Michihiko Aramaki, Rika Kosaki, Noboru Hosokai, Takao Takahashi and Kenjiro Kosaki

    Article first published online : 17 JUN 2008, DOI: 10.1002/ajmg.a.32120

  6. Molecular heterogeneity in AML/MDS patients with 3q21q26 rearrangements

    Genes, Chromosomes and Cancer

    Volume 40, Issue 3, July 2004, Pages: 179–189, Idoya Lahortiga, Iria Vázquez, Xabier Agirre, María J. Larrayoz, José L. Vizmanos, Alessandro Gozzetti, María J. Calasanz and María D. Odero

    Article first published online : 21 APR 2004, DOI: 10.1002/gcc.20033

  7. A new case of dup(3q) syndrome due to a pure duplication of 3qter

    Clinical Genetics

    Volume 62, Issue 4, October 2002, Pages: 315–320, BHW Faas, BBA De Vries, J Van Es-van Gaal, G Merkx, JMT Draaisma and DFCM Smeets

    Article first published online : 8 OCT 2002, DOI: 10.1034/j.1399-0004.2002.620411.x

  8. Exclusion of linkage to the CDL1 gene region on chromosome 3q26.3 in some familial cases of Cornelia de Lange syndrome

    American Journal of Medical Genetics

    Volume 101, Issue 2, 15 June 2001, Pages: 120–129, Ian D. Krantz, Emma Tonkin, Melanie Smith, Marcella Devoto, Armand Bottani, Claire Simpson, Mary Hofreiter, Vinod Abraham, Lori Jukofsky, Brian P. Conti, Tom Strachan and Laird Jackson

    Article first published online : 29 MAY 2001, DOI: 10.1002/1096-8628(20010615)101:2<120::AID-AJMG1319>3.0.CO;2-G

  9. Identification of breakpoint cluster regions at 1p36.3 and 3q21 in hematologic malignancies with t(1;3)(p36;q21)

    Genes, Chromosomes and Cancer

    Volume 27, Issue 3, March 2000, Pages: 229–238, Seiichi Shimizu, Kazumi Suzukawa, Takao Kodera, Toshiro Nagasawa, Tsukasa Abe, Masafumi Taniwaki, Fumiharu Yagasaki, Hideo Tanaka, Shin Fujisawa, Bertil Johansson, Tomas Ahlgren, Jun Yokota and Kazuhiro Morishita

    Article first published online : 15 FEB 2000, DOI: 10.1002/(SICI)1098-2264(200003)27:3<229::AID-GCC2>3.0.CO;2-0

  10. Clinical pre- and postnatal (step-by-step) history of a boy with unbalanced translocation—t(3;15)(q26.33;q26.1)

    American Journal of Medical Genetics Part A

    Volume 155, Issue 9, September 2011, Pages: 2320–2323, Constantinou Maria, Piotrowski Krzysztof, Zajączek Stanisław and Kałużewski Bogdan

    Article first published online : 10 AUG 2011, DOI: 10.1002/ajmg.a.34148

  11. Multipoint interphase FISH analysis of chromosome 3 abnormalities in 28 childhood AML patients

    European Journal of Haematology

    Volume 76, Issue 2, February 2006, Pages: 124–133, Irén Haltrich, Maria Kost-Alimova, Gábor Kovács, George Klein, György Fekete and Stefan Imreh

    Article first published online : 22 DEC 2005, DOI: 10.1111/j.1600-0609.2005.00576.x

  12. You have free access to this content
    Rearrangement of the BCL6 locus at 3q27 is an independent poor prognostic factor in nodal diffuse large B-cell lymphoma

    British Journal of Haematology

    Volume 117, Issue 2, May 2002, Pages: 322–332, Sharon L. Barrans, Sheila J. M. O'Connor, Paul A. S. Evans, Faith E. Davies, Roger G. Owen, Andrew P. Haynes, Gareth J. Morgan and Andrew S. Jack

    Article first published online : 25 APR 2002, DOI: 10.1046/j.1365-2141.2002.03435.x

  13. You have full text access to this OnlineOpen article
    Novel features of 3q29 deletion syndrome: Results from the 3q29 registry

    American Journal of Medical Genetics Part A

    Volume 170, Issue 4, April 2016, Pages: 999–1006, Megan R. Glassford, Jill A. Rosenfeld, Alexa A. Freedman, Michael E. Zwick, Unique Rare Chromosome Disorder Support Group and Jennifer G. Mulle

    Article first published online : 6 JAN 2016, DOI: 10.1002/ajmg.a.37537

  14. Interphase fluorescence in situ hybridization assay for the detection of 3q21 rearrangements in myeloid malignancies

    Genes, Chromosomes and Cancer

    Volume 32, Issue 4, December 2001, Pages: 373–380, Rotraud Wieser, Ulrike Schreiner, Hendrati Pirc-Danoewinata, Metin Aytekin, Helmut H. Schmidt, Harald Rieder and Christa Fonatsch

    Article first published online : 10 OCT 2001, DOI: 10.1002/gcc.1202

  15. You have free access to this content
    An interphase fluorescence in situ hybridisation assay for the detection of 3q26.2/EVI1 rearrangements in myeloid malignancies

    British Journal of Haematology

    Volume 136, Issue 6, March 2007, Pages: 806–813, Dolores Bobadilla, Elmon L. Enriquez, Georgina Alvarez, Popsie Gaytan, David Smith and Marilyn L. Slovak

    Article first published online : 2 MAR 2007, DOI: 10.1111/j.1365-2141.2007.06505.x

  16. Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: Cytogenetic and molecular analysis with delineation of the phenotype

    American Journal of Medical Genetics Part A

    Volume 136A, Issue 3, 30 July 2005, Pages: 259–264, G. Zafra de la Rosa, C.A. Venegas-Vega, N. Monroy, G. Contreras-Bucio, U. Friedrich, M. Houman, A. Saad, P. Fernández, S. Kofman-Alfaro and A. Cervantes

    Article first published online : 14 JUN 2005, DOI: 10.1002/ajmg.a.30802

  17. Duplication 3q syndrome: Molecular delineation of the critical region

    American Journal of Medical Genetics

    Volume 55, Issue 1, 2 January 1995, Pages: 33–37, Mfon S. Aqua, Patrizia Rizzu, Elizabeth A. Lindsay, Lisa G. Shaffer, Elaine H. Zackai, Joan Overhauser and Antonio Baldini

    Article first published online : 16 MAY 2005, DOI: 10.1002/ajmg.1320550111

  18. 3q29 interstitial microduplication: A new syndrome in a three-generation family

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 5, 1 March 2008, Pages: 601–609, Emily C. Lisi, Ada Hamosh, Kimberly F. Doheny, Elizabeth Squibb, Barbara Jackson, Rebecca Galczynski, George H. Thomas and Denise A.S. Batista

    Article first published online : 1 FEB 2008, DOI: 10.1002/ajmg.a.32190

  19. Patient with terminal duplication 3q and terminal deletion 5q: comparison with the 3q duplication syndrome and distal 5q deletion syndrome

    American Journal of Medical Genetics Part A

    Volume 116A, Issue 4, 1 February 2003, Pages: 376–380, Brad Angle, Frank Yen, Joseph H. Hersh and Gordon Gowans

    Article first published online : 12 DEC 2002, DOI: 10.1002/ajmg.a.10025

  20. 3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patients

    American Journal of Medical Genetics Part A

    Volume 161, Issue 12, December 2013, Pages: 3018–3022, Santina Città, Serafino Buono, Donatella Greco, Concetta Barone, Enrico Alfei, Sara Bulgheroni, Arianna Usilla, Chiara Pantaleoni and Corrado Romano

    Article first published online : 24 SEP 2013, DOI: 10.1002/ajmg.a.36142