Search Results

There are 45763 results for: content related to: Chromosomal microarray impacts clinical management

  1. You have free access to this content
    Phenotypic information in genomic variant databases enhances clinical care and research: The international standards for cytogenomic arrays consortium experience

    Human Mutation

    Volume 33, Issue 5, May 2012, Pages: 787–796, Erin Rooney Riggs, Laird Jackson, David T. Miller and Steven Van Vooren

    Version of Record online : 20 MAR 2012, DOI: 10.1002/humu.22052

  2. You have free access to this content
    Meeting the challenge of interpreting high-resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?

    BJOG: An International Journal of Obstetrics & Gynaecology

    Volume 120, Issue 5, April 2013, Pages: 594–606, D Ganesamoorthy, DL Bruno, G McGillivray, F Norris, SM White, S Adroub, DJ Amor, A Yeung, R Oertel, MD Pertile, C Ngo, AR Arvaj, S Walker, P Charan, R Palma-Dias, N Woodrow and HR Slater

    Version of Record online : 18 JAN 2013, DOI: 10.1111/1471-0528.12150

  3. You have free access to this content
    Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis

    Ultrasound in Obstetrics & Gynecology

    Volume 41, Issue 6, June 2013, Pages: 610–620, S. C. Hillman, D. J. McMullan, G. Hall, F. S. Togneri, N. James, E. J. Maher, C. H. Meller, D. Williams, R. J. Wapner, E. R. Maher and M. D. Kilby

    Version of Record online : 7 MAY 2013, DOI: 10.1002/uog.12464

  4. Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families

    Clinical Genetics

    Volume 83, Issue 1, January 2013, Pages: 23–30, M Reiff, K Ross, S Mulchandani, KJ Propert, RE Pyeritz, NB Spinner and BA Bernhardt

    Version of Record online : 18 SEP 2012, DOI: 10.1111/cge.12004

  5. You have free access to this content
    Towards a Universal Clinical Genomics Database: The 2012 International Standards for Cytogenomic Arrays Consortium Meeting

    Human Mutation

    Volume 34, Issue 6, June 2013, Pages: 915–919, Erin Rooney Riggs, Karen E. Wain, Darlene Riethmaier, Melissa Savage, Bethanny Smith-Packard, Erin B. Kaminsky, Heidi L. Rehm, Christa Lese Martin, David H. Ledbetter and W. Andrew Faucett

    Version of Record online : 2 APR 2013, DOI: 10.1002/humu.22306

  6. Prenatal chromosomal microarray analysis: a survey of prenatal genetic counselors' experiences and attitudes

    Prenatal Diagnosis

    Volume 33, Issue 4, April 2013, Pages: 371–377, Marina Mikhaelian, Patricia McCarthy Veach, Ian MacFarlane, Bonnie S. LeRoy and Matthew Bower

    Version of Record online : 1 MAR 2013, DOI: 10.1002/pd.4071

  7. Clinical aspects of prenatally detected congenital heart malformations and the yield of chromosomal microarray analysis

    Prenatal Diagnosis

    Volume 36, Issue 13, December 2016, Pages: 1185–1191, Rivka Sukenik-Halevy, Shay Sukenik, Arie Koifman, Yoav Alpert, Reli Hershkovitz, Alex Levi and Tal Biron-Shental

    Version of Record online : 29 NOV 2016, DOI: 10.1002/pd.4954

  8. You have full text access to this OnlineOpen article
    Chromosomal microarray analysis as a first-tier clinical diagnostic test: Estonian experience

    Molecular Genetics & Genomic Medicine

    Volume 2, Issue 2, March 2014, Pages: 166–175, Olga Žilina, Rita Teek, Pille Tammur, Kati Kuuse, Maria Yakoreva, Eve Vaidla, Triin Mölter-Väär, Tiia Reimand, Ants Kurg and Katrin Õunap

    Version of Record online : 9 JAN 2014, DOI: 10.1002/mgg3.57

  9. Current use of chromosomal microarray by Australian paediatricians and implications for the implementation of next generation sequencing

    Journal of Paediatrics and Child Health

    Victoria McKay, Daryl Efron, Elizabeth E Palmer, Susan M White, Chris Pearson and Margie Danchin

    Version of Record online : 27 APR 2017, DOI: 10.1111/jpc.13523

  10. You have free access to this content
    Role of chaperone-mediated autophagy in metabolism

    The FEBS Journal

    Volume 283, Issue 13, July 2016, Pages: 2403–2413, Inmaculada Tasset and Ana Maria Cuervo

    Version of Record online : 27 FEB 2016, DOI: 10.1111/febs.13677

  11. High resolution chromosomal microarray in undiagnosed neurological disorders

    Journal of Paediatrics and Child Health

    Volume 49, Issue 9, September 2013, Pages: 716–724, Katherine B Howell, Andrew J Kornberg, A Simon Harvey, Monique M Ryan, Mark T Mackay, Jeremy L Freeman, M Victoria Rodriguez Casero, Kevin J Collins, Michael Hayman, Ahmad Mohamed, Tyson L Ware, Damian Clark, Damien L Bruno, Trent Burgess, Howard Slater, George McGillivray and Richard J Leventer

    Version of Record online : 3 JUN 2013, DOI: 10.1111/jpc.12256

  12. Towards an evidence-based process for the clinical interpretation of copy number variation

    Clinical Genetics

    Volume 81, Issue 5, May 2012, Pages: 403–412, ER Riggs, DM Church, K Hanson, VL Horner, EB Kaminsky, RM Kuhn, KE Wain, ES Williams, S Aradhya, HM Kearney, DH Ledbetter, ST South, EC Thorland and CL Martin

    Version of Record online : 13 DEC 2011, DOI: 10.1111/j.1399-0004.2011.01818.x

  13. Symptoms suggestive of cow's milk allergy in infancy and pediatric inflammatory bowel disease

    Pediatric Allergy and Immunology

    Volume 27, Issue 4, June 2016, Pages: 361–367, Lauri J. Virta, Hannu Kautiainen and Kaija-Leena Kolho

    Version of Record online : 7 APR 2016, DOI: 10.1111/pai.12551

  14. You have free access to this content
    Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis

    Ultrasound in Obstetrics & Gynecology

    Volume 41, Issue 4, April 2013, Pages: 375–382, I. Mademont-Soler, C. Morales, A. Soler, J. M. MartÍnez-Crespo, Y. Shen, E. Margarit, N. Clusellas, M. Obón, B.-L. Wu and A. Sánchez

    Version of Record online : 4 MAR 2013, DOI: 10.1002/uog.12372

  15. You have full text access to this OnlineOpen article
    Loss of hepatic chaperone-mediated autophagy accelerates proteostasis failure in aging

    Aging Cell

    Volume 14, Issue 2, April 2015, Pages: 249–264, Jaime L. Schneider, Joan Villarroya, Antonio Diaz-Carretero, Bindi Patel, Aleksandra M. Urbanska, Mia M. Thi, Francesc Villarroya, Laura Santambrogio and Ana Maria Cuervo

    Version of Record online : 23 JAN 2015, DOI: 10.1111/acel.12310

  16. Chromosomal microarray use among women undergoing invasive prenatal diagnosis

    Prenatal Diagnosis

    Volume 36, Issue 7, July 2016, Pages: 656–661, Mariam Naqvi, Ilona T. Goldfarb, Kaitlin J. Hanmer and Allison Bryant

    Version of Record online : 9 JUN 2016, DOI: 10.1002/pd.4835

  17. You have free access to this content
    Chromosomal microarray in fetuses with increased nuchal translucency

    Ultrasound in Obstetrics & Gynecology

    Volume 45, Issue 1, January 2015, Pages: 95–100, I. C. B. Lund, R. Christensen, O. B. Petersen, I. Vogel and E. M. Vestergaard

    Version of Record online : 2 JAN 2015, DOI: 10.1002/uog.14726

  18. You have free access to this content
    Species-specific detection of the antiviral small-molecule compound CMA by STING

    The EMBO Journal

    Volume 32, Issue 10, May 15, 2013, Pages: 1440–1450, Taner Cavlar, Tobias Deimling, Andrea Ablasser, Karl-Peter Hopfner and Veit Hornung

    Version of Record online : 19 APR 2013, DOI: 10.1038/emboj.2013.86

  19. Cow's milk allergy as a predictor of bronchial hyperresponsiveness and airway inflammation at school age

    Clinical & Experimental Allergy

    Volume 40, Issue 10, October 2010, Pages: 1491–1497, L. P. Malmberg, K. M. Saarinen, A. S. Pelkonen, E. Savilahti and M. J. Mäkelä

    Version of Record online : 4 JUL 2010, DOI: 10.1111/j.1365-2222.2010.03567.x

  20. You have free access to this content
    Chaperone-mediated autophagy in health and disease

    FEBS Letters

    Volume 584, Issue 7, April 02, 2010, Pages: 1399–1404, Maria Kon and Ana Maria Cuervo

    Version of Record online : 22 DEC 2009, DOI: 10.1016/j.febslet.2009.12.025