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There are 9564 results for: content related to: Clinical features of Chinese patients with Huntington's disease carrying CAG repeats beyond 60 within HTT gene

  1. You have free access to this content
    Personalized gene silencing therapeutics for Huntington disease

    Clinical Genetics

    Volume 86, Issue 1, July 2014, Pages: 29–36, C. Kay, N.H. Skotte, A.L. Southwell and M.R. Hayden

    Version of Record online : 11 APR 2014, DOI: 10.1111/cge.12385

  2. Genetic aspects of Huntington's disease in Latin America. A systematic review

    Clinical Genetics

    Volume 89, Issue 3, March 2016, Pages: 295–303, R.M. Castilhos, M.C. Augustin, J.A. Santos, C. Perandones, M.L. Saraiva-Pereira, L.B. Jardim and on Behalf of Rede Neurogenética

    Version of Record online : 13 AUG 2015, DOI: 10.1111/cge.12641

  3. Prenatal testing for Huntington's disease in the Netherlands from 1998 to 2008

    Clinical Genetics

    Volume 85, Issue 1, January 2014, Pages: 78–86, MC van Rij, PAM de Koning Gans, CM Aalfs, M Elting, PF Ippel, JA Maat-Kievit, S Vermeer, CC Verschuuren-Bemelmans, MJ van Belzen, RDM Belfroid, M Losekoot, JPM Geraedts, RAC Roos, A Tibben, CEM de Die-Smulders and EK Bijlsma

    Version of Record online : 27 MAR 2013, DOI: 10.1111/cge.12090

  4. Evidence-based genetic counselling implications for Huntington disease intermediate allele predictive test results

    Clinical Genetics

    Volume 85, Issue 4, April 2014, Pages: 303–311, A. Semaka and M.R. Hayden

    Version of Record online : 15 JAN 2014, DOI: 10.1111/cge.12324

  5. Psychiatric and cognitive symptoms in Huntington's disease are modified by polymorphisms in catecholamine regulating enzyme genes

    Clinical Genetics

    Volume 89, Issue 3, March 2016, Pages: 320–327, T. Vinther-Jensen, T.T. Nielsen, E. Budtz-Jørgensen, I.U. Larsen, M.M. Hansen, L. Hasholt, L.E. Hjermind, J.E. Nielsen and A. Nørremølle

    Version of Record online : 17 JUL 2015, DOI: 10.1111/cge.12628

  6. Analysis of CAG repeats in five SCA loci in Mexican population: epidemiological evidence of a SCA7 founder effect

    Clinical Genetics

    Volume 85, Issue 2, February 2014, Pages: 159–165, J.J. Magaña, Y.S. Tapia-Guerrero, L. Velázquez-Pérez, C.M. Cerecedo-Zapata, M. Maldonado-Rodríguez, J.S. Jano-Ito, N. Leyva-García, R. González-Piña, E. Martínez-Cruz, O. Hernández-Hernández and B. Cisneros

    Version of Record online : 11 MAR 2013, DOI: 10.1111/cge.12114

  7. 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

    Version of Record online : 4 DEC 2012, DOI: 10.1111/cge.12055

  8. Spinocerebellar ataxia type 3/Machado–Joseph disease: segregation patterns and factors influencing instability of expanded CAG transmissions

    Clinical Genetics

    Volume 90, Issue 2, August 2016, Pages: 134–140, G.N. Souza, N. Kersting, A.C. Krum-Santos, A.S.P. Santos, G.V. Furtado, D. Pacheco, T.A. Gonçalves, J.A. Saute, L. Schuler-Faccini, E.P. Mattos, M.L. Saraiva-Pereira and L.B. Jardim

    Version of Record online : 3 FEB 2016, DOI: 10.1111/cge.12719

  9. Genetics of mitochondrial dysfunction and infertility

    Clinical Genetics

    L.A.M. Demain, G.S. Conway and W.G. Newman

    Version of Record online : 9 DEC 2016, DOI: 10.1111/cge.12896

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

    Clinical Genetics

    Volume 86, Issue 4, October 2014, Pages: 373–377, R.M. Castilhos, A.F.D. Souza, G.V. Furtado, T.C. Gheno, A.L. Silva, F.R. Vargas, M.-A.F.D. Lima, O. Barsottini, J.L. Pedroso, C. Godeiro Jr, D. Salarini, E.T. Pereira, K. Lin, M.-B. Toralles, J.A.M. Saute, C.R. Rieder, M. Quintas, J. Sequeiros, I. Alonso, M.L. Saraiva-Pereira and L.B. Jardim

    Version of Record online : 17 OCT 2013, DOI: 10.1111/cge.12283

  11. Chinese patients with Huntington's disease initially presenting with spinocerebellar ataxia

    Clinical Genetics

    Volume 83, Issue 4, April 2013, Pages: 380–383, Y Dong, Y-M Sun, Z-J Liu, W Ni, S-S Shi and Z-Y Wu

    Version of Record online : 26 JUL 2012, DOI: 10.1111/j.1399-0004.2012.01927.x

  12. The uptake and outcome of prenatal and pre-implantation genetic diagnosis for Huntington's disease in the Netherlands (1998–2008)

    Clinical Genetics

    Volume 85, Issue 1, January 2014, Pages: 87–95, MC van Rij, PAM de Koning Gans, MJ van Belzen, RAC Roos, JPM Geraedts, M De Rademaeker, EK Bijlsma and CEM de Die-Smulders

    Version of Record online : 21 MAR 2013, DOI: 10.1111/cge.12089

  13. Spinocerebellar ataxia: relationship between phenotype and genotype – a review

    Clinical Genetics

    Volume 90, Issue 4, October 2016, Pages: 305–314, Y.-M. Sun, C. Lu and Z.-Y. Wu

    Version of Record online : 30 JUN 2016, DOI: 10.1111/cge.12808

  14. (Epi)genotype–phenotype correlations in Beckwith–Wiedemann syndrome: a paradigm for genomic medicine

    Clinical Genetics

    Volume 89, Issue 4, April 2016, Pages: 403–415, A. Mussa, S. Russo, L. Larizza, A. Riccio and G.B. Ferrero

    Version of Record online : 30 JUL 2015, DOI: 10.1111/cge.12635

  15. Immunologic assessment and KMT2D mutation detection in Kabuki syndrome

    Clinical Genetics

    Volume 88, Issue 3, September 2015, Pages: 255–260, J.-L. Lin, W.-I. Lee, J.-L. Huang, P. K.-T. Chen, K.-C. Chan, L.-J. Lo, Y.-J. You, Y.-F. Shih, T.-Y. Tseng and M.-C. Wu

    Version of Record online : 13 OCT 2014, DOI: 10.1111/cge.12484

  16. You have full text access to this OnlineOpen article
    Funding considerations for the disclosure of genetic incidental findings in biobank research

    Clinical Genetics

    Volume 84, Issue 5, November 2013, Pages: 397–406, L Black, D Avard, MH Zawati, BM Knoppers, J Hébert, G Sauvageau and on behalf of the Leucegene Project

    Version of Record online : 10 JUN 2013, DOI: 10.1111/cge.12190

  17. Genetics of Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome

    Clinical Genetics

    L. Fontana, B. Gentilin, L. Fedele, C. Gervasini and M. Miozzo

    Version of Record online : 16 NOV 2016, DOI: 10.1111/cge.12883

  18. Molecular genetic analysis of 30 families with Joubert syndrome

    Clinical Genetics

    Volume 90, Issue 6, December 2016, Pages: 526–535, T. Suzuki, N. Miyake, Y. Tsurusaki, N. Okamoto, A. Alkindy, A. Inaba, M. Sato, S. Ito, K. Muramatsu, S. Kimura, D. Ieda, S. Saitoh, M. Hiyane, H. Suzumura, K. Yagyu, H. Shiraishi, M. Nakajima, N. Fueki, Y. Habata, Y. Ueda, Y. Komatsu, K. Yan, K. Shimoda, Y. Shitara, S. Mizuno, K. Ichinomiya, K. Sameshima, Y. Tsuyusaki, K. Kurosawa, Y. Sakai, K. Haginoya, Y. Kobayashi, C. Yoshizawa, M. Hisano, M. Nakashima, H. Saitsu, S. Takeda and N. Matsumoto

    Version of Record online : 26 SEP 2016, DOI: 10.1111/cge.12836

  19. Comprehensive review of BAP1 tumor predisposition syndrome with report of two new cases

    Clinical Genetics

    Volume 89, Issue 3, March 2016, Pages: 285–294, K. Rai, R. Pilarski, C.M. Cebulla and M.H. Abdel-Rahman

    Version of Record online : 14 JUL 2015, DOI: 10.1111/cge.12630

  20. Genetics of human Bardet–Biedl syndrome, an updates

    Clinical Genetics

    Volume 90, Issue 1, July 2016, Pages: 3–15, S.A. Khan, N. Muhammad, M.A. Khan, A. Kamal, Z.U. Rehman and S. Khan

    Version of Record online : 9 FEB 2016, DOI: 10.1111/cge.12737