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There are 8828 results for: content related to: Co-occurring conditions associated with FMR1 gene variations: Findings from a national parent survey

  1. Arithmetic difficulties in females with the fragile X premutation

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 7, 1 April 2006, Pages: 665–672, Ave M. Lachiewicz, Deborah V. Dawson, Gail A. Spiridigliozzi and Allyn McConkie-Rosell

    Version of Record online : 28 FEB 2006, DOI: 10.1002/ajmg.a.31082

  2. A distinct neurocognitive phenotype in female fragile-X premutation carriers assessed with visual attention tasks

    American Journal of Medical Genetics Part A

    Volume 116A, Issue 1, 1 January 2003, Pages: 44–51, Jean Steyaert, Eric Legius, Martine Borghgraef and Jean-Pierre Fryns

    Version of Record online : 30 AUG 2002, DOI: 10.1002/ajmg.a.10821

  3. Prevalence of CGG expansions of the FMR1 gene in a US population-based sample

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 5, July 2012, Pages: 589–597, Dr. Marsha Mailick Seltzer, Mei Wang Baker, Jinkuk Hong, Matthew Maenner, Jan Greenberg and Daniel Mandel

    Version of Record online : 22 MAY 2012, DOI: 10.1002/ajmg.b.32065

  4. Screening and instability of FMR1 alleles in a prospective sample of 24,449 mother–newborn pairs from the general population

    Clinical Genetics

    Volume 76, Issue 6, December 2009, Pages: 511–523, S Lévesque, C Dombrowski, M-L Morel, R Rehel, J-S Côté, J Bussières, K Morgan and F Rousseau

    Version of Record online : 23 OCT 2009, DOI: 10.1111/j.1399-0004.2009.01237.x

  5. Clinical involvement and protein expression in individuals with the FMR1 premutation

    American Journal of Medical Genetics

    Volume 91, Issue 2, 13 March 2000, Pages: 144–152, F. Tassone, R.J. Hagerman, A.K. Taylor, J.B. Mills, S.W. Harris, L.W. Gane and P.J. Hagerman

    Version of Record online : 4 APR 2000, DOI: 10.1002/(SICI)1096-8628(20000313)91:2<144::AID-AJMG14>3.0.CO;2-V

  6. Premature ovarian failure in the fragile X syndrome

    American Journal of Medical Genetics

    Volume 97, Issue 3, Autumn (Fall) 2000, Pages: 189–194, Stephanie L. Sherman

    Version of Record online : 12 JAN 2001, DOI: 10.1002/1096-8628(200023)97:3<189::AID-AJMG1036>3.0.CO;2-J

  7. Advances in research on the fragile X syndrome

    Mental Retardation and Developmental Disabilities Research Reviews

    Volume 6, Issue 2, 2000, Pages: 96–106, Michèle M.M. Mazzocco

    Version of Record online : 12 JUN 2000, DOI: 10.1002/1098-2779(2000)6:2<96::AID-MRDD3>3.0.CO;2-H

  8. Impact of the Fragile X mental retardation 1 (FMR1) gene premutation on neuropsychiatric functioning in adult males without fragile X-associated Tremor/Ataxia syndrome: A controlled study

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 147B, Issue 6, 5 September 2008, Pages: 859–872, Cary S. Kogan, Jeremy Turk, Randi J. Hagerman and Kim M. Cornish

    Version of Record online : 28 DEC 2007, DOI: 10.1002/ajmg.b.30685

  9. Indicators of anxiety and depression in women with the fragile X premutation: assessment of a clinical sample

    Journal of Intellectual Disability Research

    Volume 54, Issue 7, July 2010, Pages: 597–610, A. Lachiewicz, D. Dawson, G. Spiridigliozzi, M. Cuccaro, M. Lachiewicz and A. McConkie-Rosell

    Version of Record online : 14 JUN 2010, DOI: 10.1111/j.1365-2788.2010.01290.x

  10. Transcription of the FMR1 gene in individuals with fragile X syndrome

    American Journal of Medical Genetics

    Volume 97, Issue 3, Autumn (Fall) 2000, Pages: 195–203, Flora Tassone, Randi J. Hagerman, Winston D. Chamberlain and Paul J. Hagerman

    Version of Record online : 12 JAN 2001, DOI: 10.1002/1096-8628(200023)97:3<195::AID-AJMG1037>3.0.CO;2-R

  11. Newborn screening and cascade testing for FMR1 mutations

    American Journal of Medical Genetics Part A

    Volume 161, Issue 1, January 2013, Pages: 59–69, Page L. Sorensen, Louise W. Gane, Mark Yarborough, Randi J. Hagerman and Flora Tassone

    Version of Record online : 13 DEC 2012, DOI: 10.1002/ajmg.a.35680

  12. You have free access to this content
    Fragile X analysis of 1112 prenatal samples from 1991 to 2010

    Prenatal Diagnosis

    Volume 31, Issue 10, October 2011, Pages: 925–931, Sarah L. Nolin, Anne Glicksman, Xiaohua Ding, Nicole Ersalesi, W. Ted Brown, Stephanie L. Sherman and Carl Dobkin

    Version of Record online : 30 JUN 2011, DOI: 10.1002/pd.2815

  13. Paternal transmission of fragile X syndrome

    American Journal of Medical Genetics Part A

    Volume 129A, Issue 2, 30 August 2004, Pages: 184–189, Susan Zeesman, Lonnie Zwaigenbaum, Donald T. Whelan, Randi J. Hagerman, Flora Tassone and Sherryl A.M. Taylor

    Version of Record online : 29 JUN 2004, DOI: 10.1002/ajmg.a.30191

  14. Tissue-specific methylation differences in a fragile X premutation carrier

    Clinical Genetics

    Volume 55, Issue 5, May 1999, Pages: 346–352, Flora Tassone, John Longshore, Janice Zunich, Peter Steinbach, Ulrike Salat and Annette K Taylor

    Version of Record online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.1999.550508.x

  15. Reduced telomere length in individuals with FMR1 premutations and full mutations

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 5, May 2012, Pages: 1060–1065, Edmund C. Jenkins, Flora Tassone, Lingling Ye, André T. Hoogeveen, W. Ted Brown, Randi J. Hagerman and Paul J. Hagerman

    Version of Record online : 9 APR 2012, DOI: 10.1002/ajmg.a.35275

  16. You have free access to this content
    Fragile X Syndrome: The FMR1 CGG Repeat Distribution Among World Populations

    Annals of Human Genetics

    Volume 76, Issue 2, March 2012, Pages: 178–191, Emmanuel Peprah

    Version of Record online : 21 DEC 2011, DOI: 10.1111/j.1469-1809.2011.00694.x

  17. Fragile X-Linked Mental Retardation

    Standard Article

    Reviews in Cell Biology and Molecular Medicine

    Ilse Gantois, R. Frank Kooy and Ben A. Oostra

    Published Online : 15 SEP 2006, DOI: 10.1002/3527600906.mcb.200300051

  18. FMR1 gene and fragile X syndrome

    American Journal of Medical Genetics

    Volume 97, Issue 2, Summer 2000, Pages: 153–163, Barbara Bardoni, Jean-Louis Mandel and Gene S. Fisch

    Version of Record online : 28 NOV 2000, DOI: 10.1002/1096-8628(200022)97:2<153::AID-AJMG7>3.0.CO;2-M

  19. Clinical features of boys with fragile X premutations and intermediate alleles

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 121B, Issue 1, 15 August 2003, Pages: 119–127, Monica Aziz, Eleni Stathopulu, Maria Callias, Catherine Taylor, Jeremy Turk, Ben Oostra, Rob Willemsen and Mike Patton

    Version of Record online : 20 MAY 2003, DOI: 10.1002/ajmg.b.20030

  20. Mosaicism for a full mutation, premutation, and deletion of the CGG repeats results in 22% FMRP and elevated FMR1 mRNA levels in a high-functioning fragile X male

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 13, 1 July 2006, Pages: 1463–1471, Xiao-Dong Han, Berkley R. Powell, Judith L. Phalin and Farid F. Chehab

    Version of Record online : 7 JUN 2006, DOI: 10.1002/ajmg.a.31291