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There are 5220 results for: content related to: Application of chromosomal microarray in the evaluation of abnormal prenatal findings

  1. Genetic counselling difficulties and ethical implications of incidental findings from array-CGH: a 7-year national survey

    Clinical Genetics

    Volume 89, Issue 5, May 2016, Pages: 630–635, M. Lefebvre, D. Sanlaville, N. Marle, C. Thauvin-Robinet, E. Gautier, S.E. Chehadeh, A.-L. Mosca-Boidron, J. Thevenon, P. Edery, M.-P. Alex-Cordier, M. Till, S. Lyonnet, V. Cormier-Daire, J. Amiel, A. Philippe, S. Romana, V. Malan, A. Afenjar, S. Marlin, S. Chantot-Bastaraud, P. Bitoun, B. Heron, E. Piparas, F. Morice-Picard, S. Moutton, N. Chassaing, A. Vigouroux-Castera, J. Lespinasse, S. Manouvrier-Hanu, O. Boute-Benejean, C. Vincent-Delorme, F. Petit, N.L. Meur, M. Marti-Dramard, A.-M. Guerrot, A. Goldenberg, S. Redon, C. Ferrec, S. Odent, C.L. Caignec, S. Mercier, B. Gilbert-Dussardier, A. Toutain, S. Arpin, S. Blesson, I. Mortemousque, E. Schaefer, D. Martin, N. Philip, S. Sigaudy, T. Busa, C. Missirian, F. Giuliano, H.K. Benailly, P.K.V. Kien, B. Leheup, C. Benneteau, L. Lambert, R. Caumes, P. Kuentz, I. François, D. Heron, B. Keren, E. Cretin, P. Callier, S. Julia and L. Faivre

    Version of Record online : 4 JAN 2016, DOI: 10.1111/cge.12696

  2. Obtaining a genetic diagnosis in a child with disability: impact on parental quality of life

    Clinical Genetics

    Volume 89, Issue 2, February 2016, Pages: 258–266, M. Lingen, L. Albers, M. Borchers, S. Haass, J. Gärtner, S. Schröder, L. Goldbeck, R. von Kries, K. Brockmann and B. Zirn

    Version of Record online : 14 JUL 2015, DOI: 10.1111/cge.12629

  3. Array comparative genomic hybridization for diagnosis of developmental delay – an exploratory cost-consequences analysis

    Clinical Genetics

    Volume 71, Issue 3, March 2007, Pages: 254–259, WG Newman, S Hamilton, J Ayres, N Sanghera, A Smith, L Gaunt, LM Davies and J Clayton-Smith

    Version of Record online : 12 JAN 2007, DOI: 10.1111/j.1399-0004.2007.00756.x

  4. You have free access to this content
    Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysis

    Ultrasound in Obstetrics & Gynecology

    Volume 45, Issue 1, January 2015, Pages: 27–35, F. A. R. Jansen, Y. J. Blumenfeld, A. Fisher, J. M. Cobben, A. O. Odibo, A. Borrell and M. C. Haak

    Version of Record online : 2 JAN 2015, DOI: 10.1002/uog.14695

  5. Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting

    Prenatal Diagnosis

    Volume 30, Issue 12-13, December 2010, Pages: 1131–1137, Idit Maya, Bella Davidov, Liron Gershovitz, Yael Zalzstein, Ellen Taub, Justine Coppinger, Lisa G. Shaffer and Mordechai Shohat

    Version of Record online : 6 OCT 2010, DOI: 10.1002/pd.2626

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    Prenatal diagnosis using combined quantitative fluorescent polymerase chain reaction and array comparative genomic hybridization analysis as a first-line test: results from over 1000 consecutive cases

    Ultrasound in Obstetrics & Gynecology

    Volume 41, Issue 5, May 2013, Pages: 500–507, F. Scott, K. Murphy, L. Carey, W. Greville, N. Mansfield, P. Barahona, R. Robertson and A. McLennan

    Version of Record online : 22 APR 2013, DOI: 10.1002/uog.12429

  7. You have full text access to this OnlineOpen article
    Application of whole-exome sequencing for detecting copy number variants in CMT1A/HNPP

    Clinical Genetics

    Volume 90, Issue 2, August 2016, Pages: 177–181, H.-Y. Jo, M.-H. Park, H.-M. Woo, M.H. Han, B.-Y. Kim, B.-O. Choi, K.W. Chung and S.K. Koo

    Version of Record online : 4 MAR 2016, DOI: 10.1111/cge.12714

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    Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases

    Prenatal Diagnosis

    Volume 31, Issue 13, December 2011, Pages: 1270–1282, Francesco Fiorentino, Fiorina Caiazzo, Stefania Napolitano, Letizia Spizzichino, Sara Bono, Mariateresa Sessa, Andrea Nuccitelli, Anil Biricik, Anthony Gordon, Giuseppe Rizzo and Marina Baldi

    Version of Record online : 28 OCT 2011, DOI: 10.1002/pd.2884

  9. Insertional translocation detected using FISH confirmation of array-comparative genomic hybridization (aCGH) results

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 5, May 2010, Pages: 1111–1126, Sung-Hae L. Kang, Chad Shaw, Zhishuo Ou, Patricia A. Eng, M. Lance Cooper, Amber N. Pursley, Trilochan Sahoo, Carlos A. Bacino, A. Craig Chinault, Pawel Stankiewicz, Ankita Patel, James R. Lupski and Sau Wai Cheung

    Version of Record online : 25 MAR 2010, DOI: 10.1002/ajmg.a.33278

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    Microarray as a first genetic test in global developmental delay: a cost-effectiveness analysis

    Developmental Medicine & Child Neurology

    Volume 53, Issue 11, November 2011, Pages: 994–999, YANNIS TRAKADIS and MICHAEL SHEVELL

    Version of Record online : 16 AUG 2011, DOI: 10.1111/j.1469-8749.2011.04080.x

  11. Array-CGH is an effective first-tier diagnostic test for EFTUD2-associated congenital mandibulofacial dysostosis with microcephaly

    Clinical Genetics

    Volume 87, Issue 1, January 2015, Pages: 80–84, S.K. Gandomi, M. Parra, D. Reeves, V. Yap and C.-L. Gau

    Version of Record online : 20 DEC 2013, DOI: 10.1111/cge.12328

  12. Change Point Methods in Genetics

    Standard Article

    Encyclopedia of Statistical Sciences

    Jie Chen

    Published Online : 31 MAR 2010, DOI: 10.1002/0471667196.ess7126

  13. Array-Based Genomics in Glioma Research

    Brain Pathology

    Volume 20, Issue 1, January 2010, Pages: 28–38, Ahmed Idbaih, Emmanuelle Crinière, Keith L. Ligon, Olivier Delattre and Jean-Yves Delattre

    Version of Record online : 4 MAR 2009, DOI: 10.1111/j.1750-3639.2009.00274.x

  14. Prenatal diagnosis: array comparative genomic hybridization in fetuses with abnormal sonographic findings

    Acta Obstetricia et Gynecologica Scandinavica

    Volume 92, Issue 7, July 2013, Pages: 762–768, Else Marie Vestergaard, Rikke Christensen, Olav B. Petersen and Ida Vogel

    Version of Record online : 9 MAY 2013, DOI: 10.1111/aogs.12146

  15. Comparison of array comparative genomic hybridization (aCGH) to FISH and cytogenetics in prognostic evaluation of chronic lymphocytic leukemia

    International Journal of Laboratory Hematology

    Volume 33, Issue 3, June 2011, Pages: 238–244, D. P. O’MALLEY, C. GIUDICE, A. S. CHANG, D. CHANG, T. S. BARRY, M. K. HIBBARD, R. CHEN and S.-T. CHEN

    Version of Record online : 9 DEC 2010, DOI: 10.1111/j.1751-553X.2010.01284.x

  16. Change Point Methods in Genetics

    Standard Article

    Wiley StatsRef: Statistics Reference Online

    Jie Chen

    Published Online : 29 SEP 2014, DOI: 10.1002/9781118445112.stat00183

  17. Incidental findings on array comparative genomic hybridization: detection of carrier females of dystrophinopathy without any family history

    Clinical Genetics

    Volume 87, Issue 5, May 2015, Pages: 488–491, K. Nguyen, A. Putoux, T. Busa, M.P. Cordier, S. Sigaudy, M. Till, B. Chabrol, L. Michel-Calemard, R. Bernard, S. Julia, P. Malzac, A. Labalme, C. Missirian, P. Edery, C. Popovici, N. Philip and D. Sanlaville

    Version of Record online : 21 JUL 2014, DOI: 10.1111/cge.12421

  18. Diagnostic utility of array-based comparative genomic hybridization in a clinical setting

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 21, 1 November 2007, Pages: 2523–2533, Hagit N. Baris, Wen-Hann Tan, Virginia E. Kimonis and Mira B. Irons

    Version of Record online : 1 OCT 2007, DOI: 10.1002/ajmg.a.31988

  19. Analytical and clinical validity of whole-genome oligonucleotide array comparative genomic hybridization for pediatric patients with mental retardation and developmental delay

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 15, 1 August 2008, Pages: 1942–1954, Bixia Xiang, Ao Li, Dinu Valentin, Norma J. Nowak, Hongyu Zhao and Peining Li

    Version of Record online : 14 JUL 2008, DOI: 10.1002/ajmg.a.32411

  20. Clinical utility of array comparative genomic hybridization for detection of chromosomal abnormalities in pediatric acute lymphoblastic leukemia

    Pediatric Blood & Cancer

    Volume 51, Issue 2, August 2008, Pages: 171–177, Karen R. Rabin, Tsz-Kwong Man, Alexander Yu, Matthew R. Folsom, Yi-Jue Zhao, Pulivarthi H. Rao, Sharon E. Plon and Rizwan C. Naeem

    Version of Record online : 5 FEB 2008, DOI: 10.1002/pbc.21488