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There are 11886 results for: content related to: Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis

  1. You have free access to this content
    Segmental Copy-Number Variation Observed in Japanese by Array-CGH

    Annals of Human Genetics

    Volume 72, Issue 2, March 2008, Pages: 193–204, N. Takahashi, N. Tsuyama, K. Sasaki, M. Kodaira, Y. Satoh, Y. Kodama, K. Sugita and H. Katayama

    Version of Record online : 20 JAN 2008, DOI: 10.1111/j.1469-1809.2007.00415.x

  2. Clinical Significance of De Novo and Inherited Copy-Number Variation

    Human Mutation

    Volume 34, Issue 12, December 2013, Pages: 1679–1687, Anneke T. Vulto-van Silfhout, Jayne Y. Hehir-Kwa, Bregje W.M. van Bon, Janneke H.M. Schuurs-Hoeijmakers, Stephen Meader, Claudia J.M. Hellebrekers, Ilse J.M. Thoonen, Arjan P.M. de Brouwer, Han G. Brunner, Caleb Webber, Rolph Pfundt, Nicole de Leeuw and Bert B.A. de Vries

    Version of Record online : 10 OCT 2013, DOI: 10.1002/humu.22442

  3. High frequency of rare copy number variants affecting functionally related genes in patients with structural brain malformations

    Human Mutation

    Volume 32, Issue 12, December 2011, Pages: 1427–1435, Roxana Kariminejad, Allan Lind-Thomsen, Zeynep Tümer, Fikret Erdogan, Hans H. Ropers, Niels Tommerup, Reinhard Ullmann and Rikke S. Møller

    Version of Record online : 23 SEP 2011, DOI: 10.1002/humu.21585

  4. Copy number variation in the genomes of domestic animals

    Animal Genetics

    Volume 43, Issue 5, October 2012, Pages: 503–517, A. Clop, O. Vidal and M. Amills

    Version of Record online : 6 MAR 2012, DOI: 10.1111/j.1365-2052.2012.02317.x

  5. Analysis of chromosomal structural variation in patients with congenital left-sided cardiac lesions

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 100, Issue 12, December 2014, Pages: 951–964, Peter S. White, Hongbo M. Xie, Petra Werner, Joseph Glessner, Brande Latney, Hakon Hakonarson and Elizabeth Goldmuntz

    Version of Record online : 26 JUL 2014, DOI: 10.1002/bdra.23279

  6. Identification of novel gastric cancer-associated CNVs by integrated analysis of microarray

    Journal of Surgical Oncology

    Volume 102, Issue 5, 1 October 2010, Pages: 454–461, Chan-Hee Park, Sun-Young Rha, Hei-Cheul Jeung, Seung-Hui Kang, Dong-Hyuk Ki, Won-Suk Lee, Sung-Hoon Noh and Hyun-Cheol Chung

    Version of Record online : 28 APR 2010, DOI: 10.1002/jso.21585

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    Deletion Variants of RABGAP1L, 10q21.3, and C4 Are Associated With the Risk of Systemic Lupus Erythematosus in Korean Women

    Arthritis & Rheumatism

    Volume 65, Issue 4, April 2013, Pages: 1055–1063, Ji-Hong Kim, Seung-Huyn Jung, Joon Seol Bae, Hye-Soon Lee, Seon-Hee Yim, So-Yeon Park, So-Young Bang, Hae-Jin Hu, Hyoung Doo Shin, Sang-Cheol Bae and Yeun-Jun Chung

    Version of Record online : 28 MAR 2013, DOI: 10.1002/art.37854

  8. Genome-wide array-based copy number profiling in human placentas from unexplained stillbirths

    Prenatal Diagnosis

    Volume 31, Issue 10, October 2011, Pages: 932–944, R. Alan Harris, Francesca Ferrari, Shay Ben-Shachar, Xiaoling Wang, George Saade, Ignatia Van Den Veyver, Fabio Facchinetti and Kjersti Aagaard-Tillery

    Version of Record online : 5 JUL 2011, DOI: 10.1002/pd.2817

  9. Copy number variation characteristics in subpopulations of patients with autism spectrum disorders

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 156, Issue 2, March 2011, Pages: 115–124, Anna Bremer, MaiBritt Giacobini, Mats Eriksson, Peter Gustavsson, Viviann Nordin, Elisabeth Fernell, Christopher Gillberg, Ann Nordgren, Åsa Uppströmer, Britt-Marie Anderlid, Magnus Nordenskjöld and Jacqueline Schoumans

    Version of Record online : 8 DEC 2010, DOI: 10.1002/ajmg.b.31142

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    Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis

    International Journal of Cancer

    Volume 136, Issue 6, 15 March 2015, Pages: E578–E589, Sukanya Horpaopan, Isabel Spier, Alexander M. Zink, Janine Altmüller, Stefanie Holzapfel, Andreas Laner, Stefanie Vogt, Siegfried Uhlhaas, Stefanie Heilmann, Dietlinde Stienen, Sandra M. Pasternack, Kathleen Keppler, Ronja Adam, Katrin Kayser, Susanne Moebus, Markus Draaken, Franziska Degenhardt, Hartmut Engels, Andrea Hofmann, Markus M. Nöthen, Verena Steinke, Alberto Perez-Bouza, Stefan Herms, Elke Holinski-Feder, Holger Fröhlich, Holger Thiele, Per Hoffmann and Stefan Aretz

    Version of Record online : 30 SEP 2014, DOI: 10.1002/ijc.29215

  11. Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability

    Clinical Genetics

    Volume 83, Issue 2, February 2013, Pages: 145–154, Y Qiao, C Tyson, M Hrynchak, E Lopez-Rangel, J Hildebrand, S Martell, C Fawcett, L Kasmara, K Calli, C Harvard, X Liu, JJA Holden, SME Lewis and E Rajcan-Separovic

    Version of Record online : 9 APR 2012, DOI: 10.1111/j.1399-0004.2012.01860.x

  12. Copy number variations in multiple sclerosis and neuromyelitis optica

    Annals of Neurology

    Volume 78, Issue 5, November 2015, Pages: 762–774, Shinya Sato, Ken Yamamoto, Takuya Matsushita, Noriko Isobe, Yuji Kawano, Kyoko Iinuma, Masaaki Niino, Toshiyuki Fukazawa, Yuri Nakamura, Mitsuru Watanabe, Tomomi Yonekawa, Katsuhisa Masaki, Satoshi Yoshimura, Hiroyuki Murai, Ryo Yamasaki, Jun-ichi Kira and and the Japan Multiple Sclerosis Genetics Consortium

    Version of Record online : 18 SEP 2015, DOI: 10.1002/ana.24511

  13. SgD-CNV, a database for common and rare copy number variants in three Asian populations

    Human Mutation

    Volume 32, Issue 12, December 2011, Pages: 1341–1349, Haiyan Xu, Wan-Ting Poh, Xueling Sim, Rick Twee-Hee Ong, Chen Suo, Wan-Ting Tay, Chiea-Chuen Khor, Mark Seielstad, Jianjun Liu, Tin Aung, E-Shyong Tai, Tien-Yin Wong, Kee-Seng Chia and Yik-Ying Teo

    Version of Record online : 30 SEP 2011, DOI: 10.1002/humu.21601

  14. Detection of Clinically Relevant Copy Number Variants with Whole-Exome Sequencing

    Human Mutation

    Volume 34, Issue 10, October 2013, Pages: 1439–1448, Joep de Ligt, Philip M. Boone, Rolph Pfundt, Lisenka E.L.M. Vissers, Todd Richmond, Joel Geoghegan, Kathleen O'Moore, Nicole de Leeuw, Christine Shaw, Han G. Brunner, James R. Lupski, Joris A. Veltman and Jayne Y. Hehir-Kwa

    Version of Record online : 30 AUG 2013, DOI: 10.1002/humu.22387

  15. Copy number variations could predict the outcome of bortezomib plus melphalan and prednisone for initial treatment of multiple myeloma

    Genes, Chromosomes and Cancer

    Volume 54, Issue 1, January 2015, Pages: 20–27, Myungshin Kim, Shin Hyo Lee, Jiyeon Kim, Sung-Eun Lee, Yoo-Jin Kim and Chang-Ki Min

    Version of Record online : 21 AUG 2014, DOI: 10.1002/gcc.22213

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    Copy Number Variations Associated With Obesity-Related Traits in African Americans: A Joint Analysis Between GENOA and HyperGEN

    Obesity

    Volume 20, Issue 12, December 2012, Pages: 2431–2437, Wei Zhao, Nathan E. Wineinger, Hemant K. Tiwari, Thomas H. Mosley, Ulrich Broeckel, Donna K. Arnett, Sharon L.R. Kardia, Edmond K. Kabagambe and Yan V. Sun

    Version of Record online : 31 DEC 2012, DOI: 10.1038/oby.2012.162

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    Copy number variation in autoimmunity — importance hidden in complexity?

    European Journal of Immunology

    Volume 42, Issue 8, August 2012, Pages: 1969–1976, Lina M. Olsson and Rikard Holmdahl

    Version of Record online : 3 AUG 2012, DOI: 10.1002/eji.201242601

  18. Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization

    Human Mutation

    Volume 28, Issue 11, November 2007, Pages: 1124–1132, Yao-Shan Fan, Parul Jayakar, Hongbo Zhu, Deborah Barbouth, Stephanie Sacharow, Ana Morales, Virginia Carver, Paul Benke, Peter Mundy and Louis J. Elsas

    Version of Record online : 9 JUL 2007, DOI: 10.1002/humu.20581

  19. Gene copy number variation and common human disease

    Clinical Genetics

    Volume 77, Issue 3, March 2010, Pages: 201–213, M Fanciulli, E Petretto and TJ Aitman

    Version of Record online : 10 DEC 2009, DOI: 10.1111/j.1399-0004.2009.01342.x

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    Copy number variants are produced in response to low-dose ionizing radiation in cultured cells

    Environmental and Molecular Mutagenesis

    Volume 55, Issue 2, March 2014, Pages: 103–113, Martin F. Arlt, Sountharia Rajendran, Shanda R. Birkeland, Thomas E. Wilson and Thomas W. Glover

    Version of Record online : 10 DEC 2013, DOI: 10.1002/em.21840