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  1. Smith-Magenis Syndrome

    Management of Genetic Syndromes

    Ann C.M. Smith, Andrea Gropman, Pages: 739–768, 2010

    Published Online : 17 MAY 2010, DOI: 10.1002/9780470893159.ch50

  2. A large interstitial deletion of 17p13.1p11.2 involving the Smith–Magenis chromosome region in a girl with multiple congenital anomalies

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 1, 1 January 2006, Pages: 88–91, Toshiyuki Yamamoto, Hideaki Ueda, Motoyoshi Kawataki, Michiko Yamanaka, Toshihide Asou, Yuki Kondoh, Naoki Harada, Naomichi Matsumoto and Kenji Kurosawa

    Version of Record online : 6 DEC 2005, DOI: 10.1002/ajmg.a.31055

  3. Smith–Magenis syndrome and moyamoya disease in a patient with del(17)(p11.2p13.1)

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 9, 1 May 2007, Pages: 999–1008, Santhosh Girirajan, Roberto Mendoza-Londono, Christopher N. Vlangos, Lucie Dupuis, Norma J. Nowak, David J. Bunyan, Eli Hatchwell and Sarah H. Elsea

    Version of Record online : 12 APR 2007, DOI: 10.1002/ajmg.a.31689

  4. The brain finger protein gene (ZNF179), a member of the RING finger family, maps within the Smith-Magenis syndrome region at 17p11.2

    American Journal of Medical Genetics

    Volume 69, Issue 3, 31 March 1997, Pages: 320–324, Toshiyuki Kimura, Yoshiki Arakawa, Satoshi Inoue, Yoshimitsu Fukushima, Ikuko Kondo, Kumiko Koyama, Takayuki Hosoi, Akira Orimo, Masami Muramatsu, Yusuke Nakamura, Tatsuo Abe and Johji Inazawa

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19970331)69:3<320::AID-AJMG19>3.0.CO;2-T

  5. Sleep disturbance in smith-magenis syndrome (del 17 p11.2)

    American Journal of Medical Genetics

    Volume 81, Issue 2, 28 March 1998, Pages: 186–191, Ann C.M. Smith, Elizabeth Dykens and Frank Greenberg

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19980328)81:2<186::AID-AJMG11>3.0.CO;2-D

  6. Opposing phenotypes in mice with Smith–Magenis deletion and Potocki–Lupski duplication syndromes suggest gene dosage effects on fluid consumption behavior

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Pages: 2807–2814, Detlef H. Heck, Wenli Gu, Ying Cao, Shuhua Qi, Melanie Lacaria and James R. Lupski

    Version of Record online : 18 SEP 2012, DOI: 10.1002/ajmg.a.35601

  7. Prevalence, phenomenology, aetiology and predictors of challenging behaviour in Smith-Magenis syndrome

    Journal of Intellectual Disability Research

    Volume 55, Issue 2, February 2011, Pages: 138–151, J. Sloneem, C. Oliver, O. Udwin and K. A. Woodcock

    Version of Record online : 4 JAN 2011, DOI: 10.1111/j.1365-2788.2010.01371.x

  8. Regarding the Smith-Magenis syndrome multidisciplinary clinical study by Greenberg et al. [1996]

    American Journal of Medical Genetics

    Volume 73, Issue 1, 28 November 1997, Page: 97, Juan Clinton Llerena, Jr.

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19971128)73:1<97::AID-AJMG22>3.0.CO;2-L

  9. Diagnostic FISH probes for del(17)(p11.2p11.2) associated with Smith–Magenis syndrome should contain the RAI1 gene

    American Journal of Medical Genetics Part A

    Volume 132A, Issue 3, 30 January 2005, Pages: 278–282, Christopher N. Vlangos, Meredith Wilson, Jan Blancato, Ann C.M. Smith and Sarah H. Elsea

    Version of Record online : 7 DEC 2004, DOI: 10.1002/ajmg.a.30461

  10. Mosaicism for del(17) (p11.2p11.2) underlying the Smith-Magenis syndrome

    American Journal of Medical Genetics

    Volume 66, Issue 2, 11 December 1996, Pages: 193–196, Ramesh C. Juyal, Akira Kuwano, Ikuko Kondo, Federico Zara, Antonio Baldini and Pragna I. Patel

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19961211)66:2<193::AID-AJMG13>3.0.CO;2-O

  11. The prevalence and phenomenology of self-injurious and aggressive behaviour in genetic syndromes

    Journal of Intellectual Disability Research

    Volume 55, Issue 2, February 2011, Pages: 109–120, K. Arron, C. Oliver, J. Moss, K. Berg and C. Burbidge

    Version of Record online : 26 OCT 2010, DOI: 10.1111/j.1365-2788.2010.01337.x

  12. You have free access to this content
    A functional network module for Smith–Magenis syndrome

    Clinical Genetics

    Volume 75, Issue 4, April 2009, Pages: 364–374, S Girirajan, HT Truong, CL Blanchard and SH Elsea

    Version of Record online : 19 FEB 2009, DOI: 10.1111/j.1399-0004.2008.01135.x

  13. Quantitative approach to identifying abnormal variation in the human face exemplified by a study of 278 individuals with five craniofacial syndromes

    American Journal of Medical Genetics

    Volume 91, Issue 1, 6 March 2000, Pages: 8–17, Richard E. Ward, Paul L. Jamison and Judith E. Allanson

    Version of Record online : 17 MAR 2000, DOI: 10.1002/(SICI)1096-8628(20000306)91:1<8::AID-AJMG2>3.0.CO;2-#

  14. You have free access to this content
    Index

    Management of Genetic Syndromes

    Suzanne B. Cassidy, Judith E. Allanson, Pages: 925–962, 2010

    Published Online : 17 MAY 2010, DOI: 10.1002/9780470893159.index

  15. Polymorphic haplotypes of CRELD1 differentially predispose Down syndrome and euploids individuals to atrioventricular septal defect

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Pages: 2843–2848, Priyanka Ghosh, Pranami Bhaumik, Sujoy Ghosh, Umut Ozbek, Eleanor Feingold, Cheryl Maslen, Biswanath Sarkar, Vishmadeb Pramanik, Priyanka Biswas, Biswajit Bandyopadhyay and Subrata Kumar Dey

    Version of Record online : 14 SEP 2012, DOI: 10.1002/ajmg.a.35626

  16. Siblings of individuals with Smith–Magenis syndrome: an investigation of the correlates of positive and negative behavioural traits

    Journal of Intellectual Disability Research

    Volume 56, Issue 10, October 2012, Pages: 996–1007, M. S. Moshier, T. P. York, J. L. Silberg and S. H. Elsea

    Version of Record online : 7 JUN 2012, DOI: 10.1111/j.1365-2788.2012.01581.x

  17. Hemizygosity for the COP9 signalosome subunit gene, SGN3, in the Smith-Magenis syndrome

    American Journal of Medical Genetics

    Volume 87, Issue 4, 3 December 1999, Pages: 342–348, Sarah H. Elsea, Kirk Mykytyn, Katherine Ferrell, Kathryn L. Coulter, Parimal Das, Wolfgang Dubiel, Pragna I. Patel and James E. Metherall

    Version of Record online : 7 DEC 1999, DOI: 10.1002/(SICI)1096-8628(19991203)87:4<342::AID-AJMG12>3.0.CO;2-A

  18. Visual impairment due to macular disciform scars in a 20-year-old man with Smith-Magenis syndrome: Another ophthalmologic complication

    American Journal of Medical Genetics

    Volume 80, Issue 4, 4 December 1998, Pages: 373–376, Dusica Babovic-Vuksanovic, Syed M. Jalal, James A. Garrity, Dennis M. Robertson and Noralane M. Lindor

    Version of Record online : 15 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19981204)80:4<373::AID-AJMG13>3.0.CO;2-M

  19. Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)

    American Journal of Medical Genetics

    Volume 62, Issue 3, 29 March 1996, Pages: 247–254, Frank Greenberg, Richard A. Lewis, Lorraine Potocki, Daniel Glaze, Julie Parke, James Killian, Mary Ada Murphy, Daniel Williamson, Frank Brown, Robert Dutton, Charles McCluggage, Ellen Friedman, Marcelle Sulek and James R. Lupski

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19960329)62:3<247::AID-AJMG9>3.0.CO;2-Q

  20. The Smith-Magenis syndrome [del(17)p11.2]: Clinical review and molecular advances

    Mental Retardation and Developmental Disabilities Research Reviews

    Volume 2, Issue 3, 1996, Pages: 122–129, Ken-Shiung Chen, Lorraine Potocki and James R. Lupski

    Version of Record online : 7 DEC 1998, DOI: 10.1002/(SICI)1098-2779(1996)2:3<122::AID-MRDD2>3.0.CO;2-U