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There are 10104 results for: content related to: Single Nucleotide Polymorphism and FMR1 CGG Repeat Instability in Two Basque Valleys

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    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

  2. Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: A case report and review of the literature

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 10, 15 May 2008, Pages: 1358–1367, Bradford Coffee, Morna Ikeda, Dejan B. Budimirovic, Lawrence N. Hjelm, Walter E. Kaufmann and Stephen T. Warren

    Version of Record online : 15 APR 2008, DOI: 10.1002/ajmg.a.32261

  3. You have full text access to this OnlineOpen article
    Distribution of fragile X mental retardation 1 CGG repeat and flanking haplotypes in a large Chinese population

    Molecular Genetics & Genomic Medicine

    Volume 3, Issue 3, May 2015, Pages: 172–181, Wen Huang, Qiuping Xia, Shiyu Luo, Hua He, Ting Zhu, Qian Du and Ranhui Duan

    Version of Record online : 15 DEC 2014, DOI: 10.1002/mgg3.128

  4. CGG trinucleotide repeat length modulates neural plasticity and spatiotemporal processing in a mouse model of the fragile X premutation


    Volume 22, Issue 12, December 2012, Pages: 2260–2275, Michael R. Hunsaker, Kyoungmi Kim, Rob Willemsen and Robert F. Berman

    Version of Record online : 18 JUN 2012, DOI: 10.1002/hipo.22043

  5. 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

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    Genetic Diversity of the Fragile X Syndrome Gene (FMR1) in a Large Sub-Saharan West African Population

    Annals of Human Genetics

    Volume 74, Issue 4, July 2010, Pages: 316–325, Emmanuel K. Peprah, Emily G. Allen, Scott M. Williams, Laresa M. Woodard and Stephanie L. Sherman

    Version of Record online : 17 JUN 2010, DOI: 10.1111/j.1469-1809.2010.00582.x

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    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

  8. A new insight into fragile X syndrome among Basque population

    American Journal of Medical Genetics Part A

    Volume 128A, Issue 3, 30 July 2004, Pages: 250–255, Olga Peñagarikano, Alberto Gil, Mercedes Télez, Begoña Ortega, Piedad Flores, Isabel Veiga, Ana Peixoto, Begoña Criado and Isabel Arrieta

    Version of Record online : 18 MAY 2004, DOI: 10.1002/ajmg.a.30116

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    FMR1 CGG Repeat Patterns and Flanking Haplotypes in Three Asian Populations and Their Relationship With Repeat Instability

    Annals of Human Genetics

    Volume 70, Issue 6, November 2006, Pages: 784–796, Youyou Zhou, Kun Tang, Hai-Yang Law, Ivy S. L. Ng, Caroline G. L. Lee and Samuel S. Chong

    Version of Record online : 20 APR 2006, DOI: 10.1111/j.1469-1809.2006.00265.x

  10. Fragile X AGG analysis provides new risk predictions for 45–69 repeat alleles

    American Journal of Medical Genetics Part A

    Volume 161, Issue 4, April 2013, Pages: 771–778, Sarah L. Nolin, Sachin Sah, Anne Glicksman, Stephanie L. Sherman, Emily Allen, Elizabeth Berry-Kravis, Flora Tassone, Carolyn Yrigollen, Amy Cronister, Marcia Jodah, Nicole Ersalesi, Carl Dobkin, W. Ted Brown, Raghav Shroff, Gary J. Latham and Andrew G. Hadd

    Version of Record online : 26 FEB 2013, DOI: 10.1002/ajmg.a.35833

  11. A novel deletion to normal size in the sperm of a fragile X full mutation male

    Clinical Genetics

    Volume 86, Issue 3, September 2014, Pages: 295–297, S. Luo, W. Huang, C. Chen, Q. Pan, R. Duan and L. Wu

    Version of Record online : 23 OCT 2013, DOI: 10.1111/cge.12287

  12. Frequency of FMR1 premutation carriers and rate of expansion to full mutation in a retrospective diagnostic FMR1 Korean sample

    Clinical Genetics

    Volume 85, Issue 5, May 2014, Pages: 441–445, J.-H. Jang, K. Lee, E.-H. Cho, E.-H. Lee, J.-W. Kim and C.-S. Ki

    Version of Record online : 13 JUN 2013, DOI: 10.1111/cge.12195

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    The FMR1 gene and fragile X-associated tremor/ataxia syndrome

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 6, 5 September 2009, Pages: 782–798, J.R. Brouwer, R. Willemsen and B.A. Oostra

    Version of Record online : 22 DEC 2008, DOI: 10.1002/ajmg.b.30910

  14. Fragile X full mutation alleles composed of few alleles: Implications for CGG repeat expansion

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 1, 1 January 2008, Pages: 60–65, Sarah L. Nolin, Xiao-hua Ding, George E. Houck, W. Ted Brown and Carl Dobkin

    Version of Record online : 11 DEC 2007, DOI: 10.1002/ajmg.a.32087

  15. CGG repeat in the FMR1 gene: size matters

    Clinical Genetics

    Volume 80, Issue 3, September 2011, Pages: 214–225, R Willemsen, J Levenga and BA Oostra

    Version of Record online : 30 JUN 2011, DOI: 10.1111/j.1399-0004.2011.01723.x

  16. Genetic variation and evolutionary stability of the FMR1 CGG repeat in six closed human populations

    American Journal of Medical Genetics

    Volume 64, Issue 1, 12 July 1996, Pages: 220–225, Evan E. Eichler and David L. Nelson

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19960712)64:1<220::AID-AJMG40>3.0.CO;2-M

  17. Standardization of PCR amplification for fragile X trinucleotide repeat measurements

    Clinical Genetics

    Volume 61, Issue 1, January 2002, Pages: 13–20, CD O'Connell, DH Atha, JP Jakupciak, JA Amos and Kl Richie

    Version of Record online : 19 MAR 2002, DOI: 10.1034/j.1399-0004.2002.610103.x

  18. Trinucleotide Repeat Instability: Genetic Features and Molecular Mechanisms

    Brain Pathology

    Volume 7, Issue 3, July 1997, Pages: 943–963, Albert R. La Spada

    Version of Record online : 28 JAN 2008, DOI: 10.1111/j.1750-3639.1997.tb00895.x

  19. Preliminary evidence of an effect of cerebellar volume on postural sway in FMR1 premutation males

    Genes, Brain and Behavior

    Volume 14, Issue 3, March 2015, Pages: 251–259, R. C. Birch, D. R. Hocking, K. M. Cornish, J. C. Menant, N. Georgiou-Karistianis, D. E. Godler, W. Wen, A. Hackett, C. Rogers and J. N. Trollor

    Version of Record online : 25 MAR 2015, DOI: 10.1111/gbb.12204

  20. Distribution of CGG repeats and FRAXAC1/DXS548 alleles in South American populations

    American Journal of Medical Genetics

    Volume 111, Issue 3, 15 August 2002, Pages: 243–252, Regina Célia Mingroni-Netto, Claudia B. Angeli, Maria Teresa B.M. Auricchio, Emygdia R. Leal-Mesquita, Ândrea K.C. Ribeiro-dos-Santos, Iris Ferrari, Mara H. Hutz, Francisco M. Salzano, Kim Hill, A. Magdalena Hurtado and Angela M. Vianna-Morgante

    Version of Record online : 26 JUN 2002, DOI: 10.1002/ajmg.10572