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There are 6331 results for: content related to: Recombinant chromosome 7 in a mosaic 45,X/47,XXX patient

  1. Minimal clinical expression of the holoprosencephaly spectrum and of Currarino syndrome due to different cytogenetic rearrangements deleting the sonic hedgehog gene and the HLXB9 gene at 7q36.3

    American Journal of Medical Genetics Part A

    Volume 128A, Issue 1, 1 July 2004, Pages: 85–92, Denise Horn, Holger Tönnies, Heidemarie Neitzel, Dagmar Wahl, Georg Klaus Hinkel, Arpad von Moers and Oliver Bartsch

    Article first published online : 23 MAR 2004, DOI: 10.1002/ajmg.a.30031

  2. Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36

    Genes, Brain and Behavior

    Volume 12, Issue 1, February 2013, Pages: 56–69, L. L. Field, K. Shumansky, J. Ryan, D. Truong, E. Swiergala and B. J. Kaplan

    Article first published online : 7 DEC 2012, DOI: 10.1111/gbb.12003

  3. High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9

    Genes, Chromosomes and Cancer

    Volume 45, Issue 8, August 2006, Pages: 731–739, Anne R. M. von Bergh, Ellen van Drunen, Elisabeth R. van Wering, Laura J. C. M. van Zutven, Ina Hainmann, Gudmar Lönnerholm, Jules P. Meijerink, Rob Pieters and H. Berna Beverloo

    Article first published online : 27 APR 2006, DOI: 10.1002/gcc.20335

  4. You have free access to this content
    Splenic marginal zone lymphomas are characterized by loss of interstitial regions of chromosome 7q, 7q31.32 and 7q36.2 that include the protection of telomere 1 (POT1) and sonic hedgehog (SHH) genes

    British Journal of Haematology

    Volume 142, Issue 2, July 2008, Pages: 216–226, Francisco Vega, Jeong Hee Cho-Vega, Patrick A. Lennon, Madan G. Luthra, Jaime Bailey, Megan Breeden, Dan Jones, L. Jeffrey Medeiros and Rajyalakshmi Luthra

    Article first published online : 28 JUN 2008, DOI: 10.1111/j.1365-2141.2008.07176.x

  5. t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia

    Genes, Chromosomes and Cancer

    Volume 29, Issue 4, December 2000, Pages: 325–332, Sabrina Tosi, Jochen Harbott, Andrea Teigler-Schlegel, Oskar A. Haas, Hendrati Pirc-Danoewinata, Christine J. Harrison, Andrea Biondi, Giovanni Cazzaniga, Helena Kempski, Stephen W. Scherer and Lyndal Kearney

    Article first published online : 30 AUG 2000, DOI: 10.1002/1098-2264(2000)9999:9999<::AID-GCC1039>3.0.CO;2-9

  6. Cryptic 7q36.2q36.3 deletion causes multiple congenital eye anomalies and craniofacial dysmorphism

    American Journal of Medical Genetics Part A

    Volume 161, Issue 3, March 2013, Pages: 589–593, Ana Beleza-Meireles, Eunice Matoso, Lina Ramos, Joana B. Melo, Isabel M. Carreira, Eduardo D. Silva and Jorge M. Saraiva

    Article first published online : 7 FEB 2013, DOI: 10.1002/ajmg.a.35713

  7. Delineation of the phenotype associated with 7q36.1q36.2 deletion: Long QT syndrome, renal hypoplasia and mental retardation

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 9, 1 May 2008, Pages: 1195–1199, Rossella Caselli, Maria Antonietta Mencarelli, Filomena Tiziana Papa, Francesca Ariani, Ilaria Longo, Ilaria Meloni, Giuseppina Vonella, Maurizio Acampa, Alberto Auteri, Stefano Vicari, Alessandra Orsi, Giuseppe Hayek, Alessandra Renieri and Francesca Mari

    Article first published online : 17 MAR 2008, DOI: 10.1002/ajmg.a.32197

  8. Isolated postaxial polydactyly type B with mosaicism of a submicroscopic unbalanced translocation leading to an extended phenotype in offspring

    American Journal of Medical Genetics Part A

    Volume 121A, Issue 2, 30 August 2003, Pages: 168–173, Robert-Jan H. Galjaard, Herma C. van der Linde, Bert H. J. Eussen, Bert B. A. de Vries, Cokkie H. Wouters, Ben A. Oostra, Esther de Graaff and Peter Heutink

    Article first published online : 9 APR 2003, DOI: 10.1002/ajmg.a.20165

  9. Chromosome 7

    Standard Article


    Stephen W Scherer

    Published Online : 27 JAN 2006, DOI: 10.1038/npg.els.0005816

  10. Effects of deletion and duplication in a patient with a 46,XX,der(7)t(7;17)(q36;p13)mat karyotype

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 9, September 2012, Pages: 2239–2244, Anne Frühmesser, Edda Haberlandt, Werner Judmaier, Albert Schinzel, Barbara Utermann, Martin Erdel, Christine Fauth, Gerd Utermann, Johannes Zschocke and Dieter Kotzot

    Article first published online : 20 JUL 2012, DOI: 10.1002/ajmg.a.35450

  11. Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia

    Genes, Chromosomes and Cancer

    Volume 38, Issue 2, October 2003, Pages: 191–200, Sabrina Tosi, Jim Hughes, Stephen W. Scherer, Kazuhiko Nakabayashi, Jochen Harbott, Oskar A. Haas, Giovanni Cazzaniga, Andrea Biondi, Helena Kempski and Lyndal Kearney

    Article first published online : 6 AUG 2003, DOI: 10.1002/gcc.10258

  12. Homozygous feature of isolated triphalangeal thumb–preaxial polydactyly linked to 7q36: no phenotypic difference between homozygotes and heterozygotes

    Clinical Genetics

    Volume 76, Issue 1, July 2009, Pages: 85–90, CN Semerci, F Demirkan, M Özdemir, E Biskin, B Akin, H Bagci and NA Akarsu

    Article first published online : 9 JUN 2009, DOI: 10.1111/j.1399-0004.2009.01192.x

  13. Identification of active loci of a human endogenous retrovirus in neurons of patients with amyotrophic lateral sclerosis

    Annals of Neurology

    Volume 69, Issue 1, January 2011, Pages: 141–151, Renée Douville, Jiankai Liu, Jeffrey Rothstein and Avindra Nath

    Article first published online : 28 JAN 2011, DOI: 10.1002/ana.22149

  14. Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndrome

    American Journal of Medical Genetics

    Volume 102, Issue 3, 15 August 2001, Pages: 261–265, Cokkie H. Wouters, Hanne J. Meijers-Heijboer, Bert J.F.M.M. Eussen, Annette A. van der Heide, Rob B. van Luijk, Ellen van Drunen, Berna B. Beverloo, Frank Visscher and Jan O. Van Hemel

    Article first published online : 20 JUN 2001, DOI: 10.1002/ajmg.1468

  15. You have free access to this content
    High-throughput sequencing analysis of the chromosome 7q32 deletion reveals IRF5 as a potential tumour suppressor in splenic marginal-zone lymphoma

    British Journal of Haematology

    Volume 158, Issue 6, September 2012, Pages: 712–726, Vicente Fresquet, Eloy F. Robles, Anton Parker, Javier Martinez-Useros, Maria Mena, Raquel Malumbres, Xabier Agirre, Susana Catarino, David Arteta, Lourdes Osaba, Manuela Mollejo, Jesus M. Hernandez-Rivas, Maria Jose Calasanz, Masanori Daibata, Martin J.S. Dyer, Felipe Prosper, Esperanza Vizcarra, Miguel-Ángel Piris, David Oscier and Jose Angel Martinez-Climent

    Article first published online : 23 JUL 2012, DOI: 10.1111/j.1365-2141.2012.09226.x

  16. Activation of HLXB9 by juxtaposition with MYB via formation of t(6;7)(q23;q36) in an AML-M4 cell line (GDM-1)

    Genes, Chromosomes and Cancer

    Volume 42, Issue 2, February 2005, Pages: 170–178, Stefan Nagel, Maren Kaufmann, Michaela Scherr, Hans G. Drexler and Roderick A. F. MacLeod

    Article first published online : 11 NOV 2004, DOI: 10.1002/gcc.20113

  17. Risk evaluation of carriers with chromosome reciprocal translocation t(7;13)(q34;q13) and concomitant meiotic segregation analyzed by FISH on ejaculated spermatozoa

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 3, 1 February 2006, Pages: 245–256, Alina T. Midro, Ewa Wiland, Barbara Panasiuk, Ryszard Leśniewicz and Maciej Kurpisz

    Article first published online : 12 JAN 2006, DOI: 10.1002/ajmg.a.31083

  18. Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH

    American Journal of Medical Genetics Part A

    Volume 139A, Issue 3, 15 December 2005, Pages: 173–185, C. Tyson, C. Harvard, R. Locker, J.M. Friedman, S. Langlois, M.E.S. Lewis, M. Van Allen, M. Somerville, L. Arbour, L. Clarke, B. McGilivray, S.L. Yong, J. Siegel-Bartel and E. Rajcan-Separovic

    Article first published online : 10 NOV 2005, DOI: 10.1002/ajmg.a.31015

  19. Splenic marginal zone lymphoma: characterization of 7q deletion and its value in diagnosis

    The Journal of Pathology

    Volume 220, Issue 4, March 2010, Pages: 461–474, A James Watkins, Yuanxue Huang, Hongtao Ye, Estelle Chanudet, Nicola Johnson, Rifat Hamoudi, Hongxiang Liu, Gehong Dong, Ayoma Attygalle, Ellen D McPhail, Mark E Law, Peter G Isaacson, Laurence de Leval, Andrew Wotherspoon and Ming-Qing Du

    Article first published online : 30 NOV 2009, DOI: 10.1002/path.2665

  20. You have free access to this content
    Enhancer-adoption as a mechanism of human developmental disease

    Human Mutation

    Volume 32, Issue 12, December 2011, Pages: 1492–1499, Laura A. Lettice, Sarah Daniels, Elizabeth Sweeney, Shanmugasundaram Venkataraman, Paul S. Devenney, Philippe Gautier, Harris Morrison, Judy Fantes, Robert E. Hill and David R. FitzPatrick

    Article first published online : 20 OCT 2011, DOI: 10.1002/humu.21615