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There are 8842 results for: content related to: Recombinant chromosome 7 in a mosaic 45,X/47,XXX patient

  1. Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestations

    American Journal of Medical Genetics Part A

    Volume 170, Issue 4, April 2016, Pages: 896–907, Seemi Ayub, Macoura Gadji, Kada Krabchi, Sylvie Côté, Jean Gekas, Bruno Maranda and Régen Drouin

    Version of Record online : 29 JAN 2016, DOI: 10.1002/ajmg.a.37428

  2. 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

    Version of Record online : 23 MAR 2004, DOI: 10.1002/ajmg.a.30031

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    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

    Version of Record online : 7 DEC 2012, DOI: 10.1111/gbb.12003

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    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

    Version of Record online : 23 JUL 2012, DOI: 10.1111/j.1365-2141.2012.09226.x

  5. 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

    Version of Record online : 27 APR 2006, DOI: 10.1002/gcc.20335

  6. 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

    Version of Record online : 30 NOV 2009, DOI: 10.1002/path.2665

  7. A narrow deletion of 7q is common to HCL, and SMZL, but not CLL

    European Journal of Haematology

    Volume 72, Issue 6, June 2004, Pages: 390–402, Claus Lindbjerg Andersen, Alicja Gruszka-Westwood, Mette Østergaard, Jørn Koch, Elisa Jacobsen, Eigil Kjeldsen and Bendt Nielsen

    Version of Record online : 4 MAY 2004, DOI: 10.1111/j.1600-0609.2004.00243.x

  8. Duplication of 7q34 in Pediatric Low-Grade Astrocytomas Detected by High-Density Single-Nucleotide Polymorphism-Based Genotype Arrays Results in a Novel BRAF Fusion Gene

    Brain Pathology

    Volume 19, Issue 3, July 2009, Pages: 449–458, Angela J. Sievert, Eric M. Jackson, Xiaowu Gai, Hakon Hakonarson, Alexander R. Judkins, Adam C. Resnick, Leslie N. Sutton, Phillip B. Storm, Tamim H. Shaikh and Jaclyn A. Biegel

    Version of Record online : 22 OCT 2008, DOI: 10.1111/j.1750-3639.2008.00225.x

  9. A complex chromosome 7q rearrangement identified in a patient with mental retardation, anxiety disorder, and autistic features

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 2, February 2010, Pages: 427–433, Johannes G. Dauwerse, Claudia A. Ruivenkamp, Kerstin Hansson, Godfried M. Marijnissen, Dorien J.M. Peters, Martijn H. Breuning and Yvonne Hilhorst-Hofstee

    Version of Record online : 15 JAN 2010, DOI: 10.1002/ajmg.a.33203

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    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

    Version of Record online : 28 JUN 2008, DOI: 10.1111/j.1365-2141.2008.07176.x

  11. 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

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

  12. Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 5, 1 March 2006, Pages: 509–514, Susan Zeesman, Małgorzata J.M. Nowaczyk, Ikuko Teshima, Wendy Roberts, Janis Oram Cardy, Jessica Brian, Lili Senman, Lars Feuk, Lucy R. Osborne and Stephen W. Scherer

    Version of Record online : 6 FEB 2006, DOI: 10.1002/ajmg.a.31110

  13. Chromosome 7

    Standard Article


    Stephen W Scherer

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

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    Evidence for Three Novel QTLs for Adiposity on Chromosome 2 With Epistatic Interactions: The NHLBI Family Heart Study


    Volume 17, Issue 12, December 2009, Pages: 2190–2195, Mary F. Feitosa, Kari E. North, Richard H. Myers, James S. Pankow and Ingrid B. Borecki

    Version of Record online : 6 SEP 2012, DOI: 10.1038/oby.2009.181

  15. 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

    Version of Record online : 17 MAR 2008, DOI: 10.1002/ajmg.a.32197

  16. 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

    Version of Record online : 6 AUG 2003, DOI: 10.1002/gcc.10258

  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

    Version of Record online : 12 JAN 2006, DOI: 10.1002/ajmg.a.31083

  18. 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

    Version of Record online : 20 JUL 2012, DOI: 10.1002/ajmg.a.35450

  19. Elucidation of a cryptic interstitial 7q31.3 deletion in a patient with a language disorder and mild mental retardation by array-CGH

    American Journal of Medical Genetics Part A

    Volume 129A, Issue 3, 1 September 2004, Pages: 254–260, Christine Tyson, Barbara McGillivray, Chieko Chijiwa and Evica Rajcan-Separovic

    Version of Record online : 21 JUL 2004, DOI: 10.1002/ajmg.a.30245

  20. 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

    Version of Record online : 9 APR 2003, DOI: 10.1002/ajmg.a.20165