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There are 3006120 results for: content related to: Hypersociability in the behavioral phenotype of 17q21.31 microdeletion syndrome

  1. De novo triplication of the MAPT gene from the recurrent 17q21.31 microdeletion region in a patient with moderate intellectual disability and various minor anomalies

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 7, July 2012, Pages: 1765–1770, Anne Gregor, Mandy Krumbiegel, Cornelia Kraus, André Reis and Christiane Zweier

    Article first published online : 7 JUN 2012, DOI: 10.1002/ajmg.a.35427

  2. Genomic and clinical characteristics of microduplications in chromosome 17

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 5, May 2010, Pages: 1101–1110, Oleg A. Shchelochkov, S.W. Cheung and J.R. Lupski

    Article first published online : 7 APR 2010, DOI: 10.1002/ajmg.a.33248

  3. A novel de novo 1.1 Mb duplication of 17q21.33 associated with cognitive impairment and other anomalies

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 6, June 2009, Pages: 1257–1262, Farah R. Zahir, Sylvie Langlois, Kim Gall, Patrice Eydoux, Marco A. Marra and Jan M. Friedman

    Article first published online : 15 MAY 2009, DOI: 10.1002/ajmg.a.32827

  4. A novel third type of recurrent NF1 microdeletion mediated by nonallelic homologous recombination between LRRC37B-containing low-copy repeats in 17q11.2

    Human Mutation

    Volume 31, Issue 6, June 2010, Pages: 742–751, Kathrin Bengesser, David N. Cooper, Katharina Steinmann, Lan Kluwe, Nadia A. Chuzhanova, Katharina Wimmer, Marcos Tatagiba, Sigrid Tinschert, Victor-Felix Mautner and Hildegard Kehrer-Sawatzki

    Article first published online : 6 APR 2010, DOI: 10.1002/humu.21254

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    17q21 gene variation is not associated with asthma in adulthood

    Allergy

    Volume 70, Issue 1, January 2015, Pages: 107–114, E. Kreiner-Møller, D. P. Strachan, A. Linneberg, L. L. N. Husemoen, H. Bisgaard and K. Bønnelykke

    Article first published online : 10 DEC 2014, DOI: 10.1111/all.12537

  6. Common recurrent microduplication syndromes: Diagnosis and management in clinical practice

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 5, May 2010, Pages: 1066–1078, Jonathan S. Berg, Lorraine Potocki and Carlos A. Bacino

    Article first published online : 7 APR 2010, DOI: 10.1002/ajmg.a.33185

  7. Genetic variants of 17q21 are associated with childhood-onset asthma and related phenotypes in a northeastern Han Chinese population: a case–control study

    Tissue Antigens

    Volume 83, Issue 5, May 2014, Pages: 330–336, X. Yu, C. Yu, Z. Ren, Y. Deng, J. Song, H. Zhang and H. Zhou

    Article first published online : 21 MAR 2014, DOI: 10.1111/tan.12342

  8. You have free access to this content
    Asthma and atopy are associated with chromosome 17q21 markers in Chinese children

    Allergy

    Volume 64, Issue 4, April 2009, Pages: 621–628, T. F. Leung, H. Y. Sy, M. C. Y. Ng, I. H. S. Chan, G. W. K. Wong, N. L. S. Tang, M. M. Y. Waye and C. W. K. Lam

    Article first published online : 27 JAN 2009, DOI: 10.1111/j.1398-9995.2008.01873.x

  9. Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 7, October 2014, Pages: 572–580, Avinash M. Veerappa, Marita Saldanha, Prakash Padakannaya and Nallur B. Ramachandra

    Article first published online : 19 AUG 2014, DOI: 10.1002/ajmg.b.32260

  10. On the sequence-directed nature of human gene mutation: The role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease

    Human Mutation

    Volume 32, Issue 10, October 2011, Pages: 1075–1099, David N. Cooper, Albino Bacolla, Claude Férec, Karen M. Vasquez, Hildegard Kehrer-Sawatzki and Jian-Min Chen

    Article first published online : 2 SEP 2011, DOI: 10.1002/humu.21557

  11. Childhood Asthma is Associated with Polymorphic Markers of PROC on 2q14 in Addition to 17q21 Locus

    Pediatric Allergy and Immunology

    Accepted manuscript online: 19 JAN 2015, Wa Cheong Chan, Hing Yee Sy, Alice Pik-shan Kong, Chun Kwok Wong, Lai Yin Tse, Kam Lun Hon, Juliana Chung-ngor Chan, Gary Wing-kin Wong and Ting Fan Leung

    DOI: 10.1111/pai.12336

  12. Extended investigation of tau and mutation screening of other candidate genes on chromosome 17q21 in a Swedish FTDP-17 family

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 121B, Issue 1, 15 August 2003, Pages: 112–118, Susanne Froelich Fabre, Pia Axelman, Åsa Almkvist, Hans Basun and Lars Lannfelt

    Article first published online : 9 JUN 2003, DOI: 10.1002/ajmg.b.20067

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    Genome-wide association studies for discovery of genes involved in asthma

    Respirology

    Volume 16, Issue 3, April 2011, Pages: 396–406, LOUBNA AKHABIR and ANDREW J. SANDFORD

    Article first published online : 30 MAR 2011, DOI: 10.1111/j.1440-1843.2011.01939.x

  14. You have free access to this content
    The Human Obesity Gene Map: The 2005 Update

    Obesity

    Volume 14, Issue 4, April 2006, Pages: 529–644, Tuomo Rankinen, Aamir Zuberi, Yvon C. Chagnon, S. John Weisnagel, George Argyropoulos, Brandon Walts, Louis Pérusse and Claude Bouchard

    Article first published online : 6 SEP 2012, DOI: 10.1038/oby.2006.71

  15. The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes

    Prenatal Diagnosis

    Volume 31, Issue 8, August 2011, Pages: 778–787, Lisa G. Shaffer, Justine Coppinger, S. Annie Morton, Sarah Alliman, Jessica Burleson, Ryan Traylor, Cathryn Walker, Steve Byerly, Allen N. Lamb, Roger Schultz, J. Britt Ravnan, Catherine D. Kashork, Beth S. Torchia, Scott Sulpizio, Kyle Sundin, Mack Schermer, Karl Adler, Stephanie Dallaire and Blake C. Ballif

    Article first published online : 21 JUN 2011, DOI: 10.1002/pd.2766

  16. Allelic loss at 1p34, 13q12, 17p13.3, and 17q21.1 correlates with poor postoperative prognosis in breast cancer

    Genes, Chromosomes and Cancer

    Volume 26, Issue 2, October 1999, Pages: 134–141, Mitsuru Emi, Masataka Yoshimoto, Takaaki Sato, Satoshi Matsumoto, Yoshihito Utada, Isao Ito, Kaori Minobe, Takuji Iwase, Toyomasa Katagiri, Kouichi Bando, Futoshi Akiyama, Yousuke Harada, Kouichi Fukino, Goi Sakamoto, Mieko Matsushima, Aritoshi Iida, Takashi Tada, Hiroko Saito, Yoshio Miki, Fujio Kasumi and Yusuke Nakamura

    Article first published online : 31 AUG 1999, DOI: 10.1002/(SICI)1098-2264(199910)26:2<134::AID-GCC5>3.0.CO;2-9

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    Comparative genomic hybridization (CGH) analysis of stage 4 neuroblastoma reveals high frequency of 11q deletion in tumors lacking MYCN amplification

    International Journal of Cancer

    Volume 91, Issue 5, 1 March 2001, Pages: 680–686, D. Plantaz, J. Vandesompele, N. Van Roy, M. Łastowska, N. Bown, V. Combaret, M.C. Favrot, O. Delattre, J. Michon, J. Bénard, O. Hartmann, J.C. Nicholson, F.M. Ross, C. Brinkschmidt, G. Laureys, H. Caron, K.K. Matthay, B.G. Feuerstein and F. Speleman

    Article first published online : 20 MAR 2001, DOI: 10.1002/1097-0215(200002)9999:9999<::AID-IJC1114>3.0.CO;2-R

  18. Whole-genome array-CGH identifies novel contiguous gene deletions and duplications associated with developmental delay, mental retardation, and dysmorphic features

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 13, 1 July 2007, Pages: 1431–1441, Swaroop Aradhya, Melanie A. Manning, Alessandra Splendore and Athena M. Cherry

    Article first published online : 13 JUN 2007, DOI: 10.1002/ajmg.a.31773

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    Genetic studies of 457 breast cancers. Clinicopathologic parameters compared with genetic alterations

    Cancer

    Volume 74, Issue 8, 15 October 1994, Pages: 2281–2286, Yousuke Harada, Toyomasa Katagiri, Isao Ito, Yusuke Nakamura, Mitsuru Emi, Futoshi Akiyama, Goi Sakamoto and Fujio Kasumi

    Article first published online : 28 JUN 2006, DOI: 10.1002/1097-0142(19941015)74:8<2281::AID-CNCR2820740812>3.0.CO;2-I

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    Variants in the 17q21 asthma susceptibility locus are associated with allergic rhinitis in the Japanese population

    Allergy

    Volume 68, Issue 1, January 2013, Pages: 92–100, K. Tomita, M. Sakashita, T. Hirota, S. Tanaka, K. Masuyama, T. Yamada, S. Fujieda, A. Miyatake, N. Hizawa, M. Kubo, Y. Nakamura and M. Tamari

    Article first published online : 12 NOV 2012, DOI: 10.1111/all.12066