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There are 33185 results for: content related to: Analysis of CAG repeats in five SCA loci in Mexican population: epidemiological evidence of a SCA7 founder effect

  1. Large normal alleles and SCA2 prevalence: lessons from a nationwide study and analysis of the literature

    Clinical Genetics

    Volume 86, Issue 1, July 2014, Pages: 96–98, J.M. Laffita-Mesa, L.E. Almaguer-Mederos, V. Kourí, P.O. Bauer, Y. Vázquez-Mojena, T. Cruz Mariño and L. Velázquez-Pérez

    Article first published online : 18 JUL 2013, DOI: 10.1111/cge.12221

  2. The Cuban program for predictive testing of SCA2: 11 years and 768 individuals to learn from

    Clinical Genetics

    Volume 83, Issue 6, June 2013, Pages: 518–524, T Cruz-Mariño, L Velázquez-Pérez, Y González-Zaldivar, R Aguilera-Rodríguez, M Velázquez-Santos, Y Vázquez-Mojena, A Estupiñán-Rodríguez, JM Laffita-Mesa, R Reynaldo-Armiñán, LE Almaguer-Mederos and M Paneque

    Article first published online : 23 APR 2013, DOI: 10.1111/cge.12142

  3. A selective sweep in a microsporidian parasite Nosema-tolerant honeybee population, Apis mellifera

    Animal Genetics

    Volume 45, Issue 2, April 2014, Pages: 267–273, Q. Huang, H. M. G. Lattorff, P. Kryger, Y. Le Conte and R. F. A. Moritz

    Article first published online : 10 DEC 2013, DOI: 10.1111/age.12114

  4. Huntington disease and Huntington disease-like in a case series from Brazil

    Clinical Genetics

    RM Castilhos, AFD Souza, GV Furtado, TC Gheno, AL Silva, FR Vargas, M-AFD Lima, O Barsottini, JL Pedroso, C Godeiro Jr, D Salarini, ET Pereira, K Lin, M-B Toralles, JAM Saute, CR Rieder, M Quintas, J Sequeiros, I Alonso, ML Saraiva-Pereira and LB Jardim

    Article first published online : 17 OCT 2013, DOI: 10.1111/cge.12283

  5. Exome sequencing identifies UPF3B as the causative gene for a Chinese non-syndrome mental retardation pedigree

    Clinical Genetics

    Volume 83, Issue 6, June 2013, Pages: 560–564, X Xu, L Zhang, P Tong, G Xun, W Su, Z Xiong, T Zhu, Y Zheng, S Luo, Y Pan, K Xia and Z Hu

    Article first published online : 28 SEP 2012, DOI: 10.1111/cge.12014

  6. Excessively redundant umbilical skin as a potential early clinical feature of Morquio syndrome and FKBP14-related Ehlers–Danlos syndrome

    Clinical Genetics

    A.A. Aldeeri, A.M. Alazami, H. Hijazi, F. Alzahrani and F.S. Alkuraya

    Article first published online : 22 MAY 2014, DOI: 10.1111/cge.12414

  7. Proteus syndrome review: molecular, clinical, and pathologic features

    Clinical Genetics

    Volume 85, Issue 2, February 2014, Pages: 111–119, M. Michael Cohen Jr.

    Article first published online : 23 OCT 2013, DOI: 10.1111/cge.12266

  8. The Birth, Death, and Persistence of Firms: Creative Destruction and the Spatial Distribution of U.S. Manufacturing Establishments, 2000–2006

    Economic Geography

    Volume 89, Issue 3, July 2013, Pages: 203–226, Jason P. Brown, Dayton M. Lambert and Raymond J. G. M. Florax

    Article first published online : 5 APR 2013, DOI: 10.1111/ecge.12014

  9. Making headway with genetic diagnostics of intellectual disabilities

    Clinical Genetics

    Volume 85, Issue 2, February 2014, Pages: 101–110, M.H. Willemsen and T. Kleefstra

    Article first published online : 25 AUG 2013, DOI: 10.1111/cge.12244

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    The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings

    Clinical Genetics

    Volume 84, Issue 4, October 2013, Pages: 303–314, FC Connell, K Gordon, G Brice, V Keeley, S Jeffery, PS Mortimer, S Mansour and P Ostergaard

    Article first published online : 27 JUN 2013, DOI: 10.1111/cge.12173

  11. Human facial dysostoses

    Clinical Genetics

    Volume 83, Issue 6, June 2013, Pages: 499–510, D Wieczorek

    Article first published online : 8 APR 2013, DOI: 10.1111/cge.12123

  12. Genetic parameters and across-line SNP associations differ for natural antibody isotypes IgM and IgG in laying hens

    Animal Genetics

    Volume 44, Issue 4, August 2013, Pages: 413–424, Y. Sun, F. Biscarini, H. Bovenhuis, H. K. Parmentier and J. J. van der Poel

    Article first published online : 12 DEC 2012, DOI: 10.1111/age.12014

  13. You have free access to this content
    Genetics of the corneal endothelial dystrophies: an evidence-based review

    Clinical Genetics

    Volume 84, Issue 2, August 2013, Pages: 109–119, A J Aldave, J Han and R F Frausto

    Article first published online : 10 JUN 2013, DOI: 10.1111/cge.12191

  14. Epigenetic changes in diabetes

    Clinical Genetics

    Volume 84, Issue 1, July 2013, Pages: 1–10, ST Keating and A El-Osta

    Article first published online : 11 MAR 2013, DOI: 10.1111/cge.12121

  15. Epigenetic mechanisms in the pathogenesis of Lynch syndrome

    Clinical Genetics

    Volume 85, Issue 5, May 2014, Pages: 403–412, P. Peltomäki

    Article first published online : 17 FEB 2014, DOI: 10.1111/cge.12349

  16. The genetics of type 2 diabetes and its clinical relevance

    Clinical Genetics

    Volume 83, Issue 4, April 2013, Pages: 297–306, A Pal and MI McCarthy

    Article first published online : 4 DEC 2012, DOI: 10.1111/cge.12055

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    Detection of novel genetic variation in autosomal dominant retinitis pigmentosa

    Clinical Genetics

    Volume 84, Issue 5, November 2013, Pages: 441–452, E Borràs, M de Sousa Dias, I Hernan, B Pascual, B Mañé, MJ Gamundi, B Delás and M Carballo

    Article first published online : 15 APR 2013, DOI: 10.1111/cge.12151

  18. Unmasking Kabuki syndrome

    Clinical Genetics

    Volume 83, Issue 3, March 2013, Pages: 201–211, N Bögershausen and B Wollnik

    Article first published online : 26 NOV 2012, DOI: 10.1111/cge.12051

  19. Clinical and genetic heterogeneity of amyotrophic lateral sclerosis

    Clinical Genetics

    Volume 83, Issue 5, May 2013, Pages: 408–416, M Sabatelli, A Conte and M Zollino

    Article first published online : 12 MAR 2013, DOI: 10.1111/cge.12117

  20. Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype

    Clinical Genetics

    I Filges, E Nosova, E Bruder, S Tercanli, K Townsend, WT Gibson, B Röthlisberger, K Heinimann, JG Hall, CY Gregory-Evans, WW Wasserman, P Miny and JM Friedman

    Article first published online : 18 NOV 2013, DOI: 10.1111/cge.12301