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There are 2749 results for: content related to: DNA fingerprinting tags novel altered chromosomal regions and identifies the involvement of SOX5 in the progression of prostate cancer

  1. Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features

    Human Mutation

    Volume 33, Issue 4, April 2012, Pages: 728–740, Allen N. Lamb, Jill A. Rosenfeld, Nicholas J. Neill, Michael E. Talkowski, Ian Blumenthal, Santhosh Girirajan, Debra Keelean-Fuller, Zheng Fan, Jill Pouncey, Cathy Stevens, Loren Mackay-Loder, Deborah Terespolsky, Patricia I. Bader, Kenneth Rosenbaum, Stephanie E. Vallee, John B. Moeschler, Roger Ladda, Susan Sell, Judith Martin, Shawnia Ryan, Marilyn C. Jones, Rocio Moran, Amy Shealy, Suneeta Madan-Khetarpal, Juliann McConnell, Urvashi Surti, Andrée Delahaye, Bénédicte Heron-Longe, Eva Pipiras, Brigitte Benzacken, Sandrine Passemard, Alain Verloes, Bertrand Isidor, Cedric Le Caignec, Gwen M. Glew, Kent E. Opheim, Maria Descartes, Evan E. Eichler, Cynthia C. Morton, James F. Gusella, Roger A. Schultz, Blake C. Ballif and Lisa G. Shaffer

    Article first published online : 12 MAR 2012, DOI: 10.1002/humu.22037

  2. A father and son with mental retardation, a characteristic face, inv(12), and insertion trisomy 12p12.3-p11.2

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 3, 1 February 2006, Pages: 238–244, Desheng Liang, Lingqian Wu, Qian Pan, Naoki Harada, Zhigao Long, Kun Xia, Koh-ichiro Yoshiura, Heping Dai, Norio Niikawa, Fang Cai and Jiahui Xia

    Article first published online : 12 JAN 2006, DOI: 10.1002/ajmg.a.31077

  3. A Meniere's disease gene linked to chromosome 12p12.3

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 141B, Issue 5, 5 July 2006, Pages: 463–467, Joakim Klar, Carina Frykholm, Ulla Friberg and Niklas Dahl

    Article first published online : 1 JUN 2006, DOI: 10.1002/ajmg.b.30347

  4. Abnormalities of the der(12)t(12;21) in ETV6-RUNX1 acute lymphoblastic leukemia

    Genes, Chromosomes and Cancer

    Volume 52, Issue 2, February 2013, Pages: 202–213, Halima Al-Shehhi, Zoe J. Konn, Claire J. Schwab, Amy Erhorn, Kerry E. Barber, Sarah L. Wright, Alem S. Gabriel, Christine J. Harrison and Anthony V. Moorman

    Article first published online : 18 OCT 2012, DOI: 10.1002/gcc.22021

  5. Construction of tree models for pathogenesis of nasopharyngeal carcinoma

    Genes, Chromosomes and Cancer

    Volume 40, Issue 4, August 2004, Pages: 307–315, Zhongxi Huang, Richard Desper, Alejandro A. Schäffer, Zhihua Yin, Xin Li and Kaitai Yao

    Article first published online : 11 MAY 2004, DOI: 10.1002/gcc.20036

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    Expression mapping at 12p12-13 in advanced prostate carcinoma

    International Journal of Cancer

    Volume 109, Issue 5, 1 May 2004, Pages: 668–672, Adam S. Kibel, John Huagen, Chan Guo, William B. Isaacs, Yan Yan, Kenneth J. Pienta and Paul J. Goodfellow

    Article first published online : 22 JAN 2004, DOI: 10.1002/ijc.20060

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    Whole-genome screening for susceptibility genes in multicase families with Behçet's disease

    Arthritis & Rheumatism

    Volume 52, Issue 6, June 2005, Pages: 1836–1842, Jumana Karasneh, Ahmet Gül, William E. Ollier, Alan J. Silman and Jane Worthington

    Article first published online : 2 JUN 2005, DOI: 10.1002/art.21060

  8. Familial cryptic translocation with del 4q34[RIGHTWARDS ARROW]qter and dup 12pter[RIGHTWARDS ARROW]p13 in sibs with tracheal stenosis: Clinical, classical and molecular cytogenetic studies and CGH analyses from archival placental tissues evidencing tertiary trisomy 4 in one abortion specimen

    American Journal of Medical Genetics

    Volume 94, Issue 4, 2 October 2000, Pages: 271–280, Barbara Fritz, Susanne Greber-Platzer, Thomas Frischer, Berthold Streubel, Johann Gröblacher, Gabriele Amann, Pavel Ventruba, Helga Rehder and Christa Fonatsch

    Article first published online : 13 OCT 2000, DOI: 10.1002/1096-8628(20001002)94:4<271::AID-AJMG2>3.0.CO;2-Y

  9. A 10.46 Mb 12p11.1–12.1 interstitial deletion coincident with a 0.19 Mb NRXN1 deletion detected by array CGH in a girl with scoliosis and autism

    American Journal of Medical Genetics Part A

    Volume 155, Issue 7, July 2011, Pages: 1745–1752, Yasemin Soysal, Joris Vermeesch, Nooshin Ardeshir Davani, Kuyaş Hekimler and Necat İmirzalıoğlu

    Article first published online : 27 MAY 2011, DOI: 10.1002/ajmg.a.34101

  10. 12p12-13 deletion in prostate tumors and quantitative expression of CDKN1B and ETV6 candidate genes

    Genes, Chromosomes and Cancer

    Volume 31, Issue 2, June 2001, Pages: 199–200, Alain Latil, Marc Guérard, Philippe Berthon and Olivier Cussenot

    Article first published online : 2 APR 2001, DOI: 10.1002/gcc.1135

  11. A girl with distinctive features of borderline high blood pressure, short stature, characteristic brachydactyly, and 11.47 Mb deletion in 12p11.21–12p12.2 by oligonucleotide array CGH

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 10, October 2009, Pages: 2321–2323, Hong-Yong Lu, Ying-Xia Cui, Yi-Chao Shi, Xin-Yi Xia, Quan Liang, Bing Yao, Yi-Feng Ge, Xiao-Jun Li and Yu-Feng Huang

    Article first published online : 16 SEP 2009, DOI: 10.1002/ajmg.a.33030

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    Loss of heterozygosity of chromosome 12p does not correlate with KRAS mutation in non-small cell lung cancer

    International Journal of Cancer

    Volume 107, Issue 6, 20 December 2003, Pages: 962–969, Mika Uchiyama, Noriyasu Usami, Masashi Kondo, Shoichi Mori, Masao Ito, Genshi Ito, Hiromu Yoshioka, Munehisa Imaizumi, Yuichi Ueda, Masahide Takahashi, John D. Minna, Kaoru Shimokata and Yoshitaka Sekido

    Article first published online : 18 SEP 2003, DOI: 10.1002/ijc.11493

  13. Molecular characterization of a balanced rearrangement of chromosome 12 in two siblings with Noonan syndrome

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 12, December 2009, Pages: 2723–2730, Svetlana A. Yatsenko, Maria del Valle Torrado, Priscilla H. Fernandes, Joanna Wiszniewska, Marta Gallego, Jorge Herrera and Carlos A. Bacino

    Article first published online : 24 NOV 2009, DOI: 10.1002/ajmg.a.33112

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    Identification of transcripts modulated by ETV6 expression

    British Journal of Haematology

    Volume 136, Issue 1, January 2007, Pages: 48–62, Gino Boily, Josiane Larose, Sylvie Langlois and Daniel Sinnett

    Article first published online : 27 OCT 2006, DOI: 10.1111/j.1365-2141.2006.06377.x

  15. Deletion mapping at 12p12–13 in metastatic prostate cancer

    Genes, Chromosomes and Cancer

    Volume 25, Issue 3, July 1999, Pages: 270–276, Adam S. Kibel, Diha Freije, William B. Isaacs and G. Steven Bova

    Article first published online : 28 MAY 1999, DOI: 10.1002/(SICI)1098-2264(199907)25:3<270::AID-GCC9>3.0.CO;2-Z

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    Correlation of cytogenetic, molecular cytogenetic, and clinical findings in 59 patients with ANLL or MDS and abnormalities of the short arm of chromosome 12

    British Journal of Haematology

    Volume 100, Issue 3, March 1998, Pages: 521–533, Berthold Streubel, Cristina Sauerland, Gerhard Heil, Mathias Freund, Heinrich Bartels, Eva Lengfelder, Hannes Wandt, Wolf-Dieter Ludwig, Hadwiga Nowotny, Michael Baldus, Bernward Grothaus-Pinke, Thomas Büchner and Christa Fonatsch

    Article first published online : 25 DEC 2001, DOI: 10.1046/j.1365-2141.1998.00591.x

  17. Molecular cytogenetic analysis of a constitutional de novo interstitial deletion of chromosome 12p in a boy with developmental delay and congenital anomalies

    American Journal of Medical Genetics Part A

    Volume 116A, Issue 1, 1 January 2003, Pages: 66–70, Birgitta Gläser, Eva Rossier, Gotthold Barbi, Loredana Delle Chiaie, Christian Blank, Walther Vogel and Hildegard Kehrer-Sawatzki

    Article first published online : 30 AUG 2002, DOI: 10.1002/ajmg.a.10878

  18. Sox5 controls dorsal progenitor and interneuron specification in the spinal cord

    Developmental Neurobiology

    Alejandra C. Quiroga, C. Claus Stolt, Ruth Diez del Corral, Spas Dimitrov, Siro Pérez-Alcalá, Elisabeth Sock, Julio A. Barbas, Michael Wegner and Aixa V. Morales

    Article first published online : 13 NOV 2014, DOI: 10.1002/dneu.22240

  19. Familial interstitial deletion 11(p11.12p12) associated with parietal foramina, brachymicrocephaly, and mental retardation

    American Journal of Medical Genetics

    Volume 45, Issue 5, 1 March 1993, Pages: 581–583, Lisa G. Shaffer, Jacqueline T. Hecht, David H. Ledbetter and Dr. Frank Greenberg

    Article first published online : 7 JUN 2005, DOI: 10.1002/ajmg.1320450512

  20. Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 153B, Issue 2, March 2010, Pages: 503–511, Kerstin U. Ludwig, Darina Roeske, Stefan Herms, Johannes Schumacher, Andreas Warnke, Ellen Plume, Nina Neuhoff, Jennifer Bruder, Helmut Remschmidt, Gerd Schulte-Körne, Bertram Müller-Myhsok, Markus M. Nöthen and Per Hoffmann

    Article first published online : 9 JUL 2009, DOI: 10.1002/ajmg.b.31007