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There are 3828 results for: content related to: Prenatal testing for Huntington's disease in the Netherlands from 1998 to 2008

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    Recommendations for the predictive genetic test in Huntington's disease

    Clinical Genetics

    Volume 83, Issue 3, March 2013, Pages: 221–231, R MacLeod, A Tibben, M Frontali, G Evers-Kiebooms, A Jones, A Martinez-Descales, RA Roos and Editorial Committee and Working Group ‘Genetic Testing Counselling’ of the European Huntington Disease Network

    Version of Record online : 29 JUL 2012, DOI: 10.1111/j.1399-0004.2012.01900.x

  2. Predictive testing for Huntington disease: interpretation and significance of intermediate alleles

    Clinical Genetics

    Volume 70, Issue 4, October 2006, Pages: 283–294, A Semaka, S Creighton, S Warby and MR Hayden

    Version of Record online : 21 AUG 2006, DOI: 10.1111/j.1399-0004.2006.00668.x

    Corrected by:

    Corrigendum

    Vol. 71, Issue 1, 99, Version of Record online: 14 DEC 2006

  3. Large normal and reduced penetrance alleles in Huntington disease: instability in families and frequency at the laboratory, at the clinic and in the population

    Clinical Genetics

    Volume 78, Issue 4, October 2010, Pages: 381–387, J Sequeiros, EM Ramos, J Cerqueira, MC Costa, A Sousa, J Pinto-Basto and I Alonso

    Version of Record online : 11 FEB 2010, DOI: 10.1111/j.1399-0004.2010.01388.x

  4. Unstable familial transmissions of Huntington disease alleles with 27–35 CAG repeats (intermediate alleles)

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 153B, Issue 1, January 2010, Pages: 314–320, A. Semaka, J.A. Collins and M.R. Hayden

    Version of Record online : 19 MAY 2009, DOI: 10.1002/ajmg.b.30970

  5. Experience in prenatal testing for Huntington's disease in The Netherlands: procedures, results and guidelines (1987–1997)

    Prenatal Diagnosis

    Volume 19, Issue 5, May 1999, Pages: 450–457, Anneke Maat-Kievit, Maria Vegter-van der Vlis, Moniek Zoeteweij, Monique Losekoot, Arie van Haeringen, Humphrey Kanhai and Raymund Roos

    Version of Record online : 26 MAY 1999, DOI: 10.1002/(SICI)1097-0223(199905)19:5<450::AID-PD568>3.0.CO;2-L

  6. 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

  7. Using a roster and haplotyping is useful in risk assessment for persons with intermediate and reduced penetrance alleles in Huntington disease

    American Journal of Medical Genetics

    Volume 105, Issue 8, 8 December 2001, Pages: 737–744, Anneke Maat-Kievit, Paula Helderman-van den Enden, Monique Losekoot, Peter de Knijff, René Belfroid, Maria Vegter-van der Vlis, Raymund Roos and Martijn Breuning

    Version of Record online : 30 OCT 2001, DOI: 10.1002/ajmg.1610

  8. 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

  9. Predictive testing of 25 percent at-risk individuals for Huntington disease (1987–1997)

    American Journal of Medical Genetics

    Volume 88, Issue 6, 15 December 1999, Pages: 662–668, Anneke Maat-Kievit, Maria Vegter-van der Vlis, Moniek Zoeteweij, Monique Losekoot, Arie van Haeringen and Raymund A.C. Roos

    Version of Record online : 20 APR 2000, DOI: 10.1002/(SICI)1096-8628(19991215)88:6<662::AID-AJMG16>3.0.CO;2-A

  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. Intergeneration CAG expansion and contraction in a Chinese HD family

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 141B, Issue 3, 5 April 2006, Pages: 242–244, Yanping Tang, Ying Wang, Ping Yang, Yuan Liu, Bo Wang, Robert Podolsky, Richard McIndoe and Cong-Yi Wang

    Version of Record online : 8 MAR 2006, DOI: 10.1002/ajmg.b.30261

  12. High frequency of intermediate alleles on huntington disease-associated haplotypes in British Columbia's general population

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 8, December 2013, Pages: 864–871, Alicia Semaka, Chris Kay, Crystal N. Doty, Jennifer A. Collins, Natalie Tam and Michael R. Hayden

    Version of Record online : 30 AUG 2013, DOI: 10.1002/ajmg.b.32193

  13. New Huntington disease mutation arising from a paternal CAG34 allele showing somatic length variation in serially passaged lymphoblasts

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 133B, Issue 1, 5 February 2005, Pages: 127–130, Milena Cannella, Vittorio Maglione, Tiziana Martino, Maria Simonelli, Giuseppe Ragona and Ferdinando Squitieri

    Version of Record online : 15 NOV 2004, DOI: 10.1002/ajmg.b.30125

  14. Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000

    Clinical Genetics

    Volume 63, Issue 6, June 2003, Pages: 462–475, S Creighton, EW Almqvist, D MacGregor, B Fernandez, H Hogg, J Beis, JP Welch, C Riddell, R Lokkesmoe, M Khalifa, J MacKenzie, A Sajoo, S Farrell, F Robert, A Shugar, A Summers, W Meschino, D Allingham-Hawkins, T Chiu, A Hunter, J Allanson, H Hare, J Schween, L Collins, S Sanders, C Greenberg, S Cardwell, E Lemire, P MacLeod and MR Hayden

    Version of Record online : 3 JUN 2003, DOI: 10.1034/j.1399-0004.2003.00093.x

  15. 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

  16. A Complete Association of an intronic SNP rs6798742 with Origin of Spinocerebellar Ataxia Type 7-CAG Expansion Loci in the Indian and Mexican Population

    Annals of Human Genetics

    Mohammed Faruq, Jonathan J. Magaña, Varun Suroliya, Ankita Narang, Nadia M. Murillo-Melo, Oscar Hernández-Hernández, Achal K. Srivastava and Mitali Mukerji

    Version of Record online : 9 JUN 2017, DOI: 10.1111/ahg.12200

  17. An intergenerational contraction of a fully penetrant Huntington disease allele to a reduced penetrance allele: Interpretation of results and significance for risk assessment and genetic counseling

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 4, April 2009, Pages: 732–736, Fatimah Nahhas, James Garbern, Shawna Feely and Gerald L. Feldman

    Version of Record online : 6 MAR 2009, DOI: 10.1002/ajmg.a.32720

  18. Huntington's disease

    Prenatal Diagnosis

    Volume 16, Issue 13, December 1996, Pages: 1237–1245, David Craufurd

    Version of Record online : 4 DEC 1998, DOI: 10.1002/(SICI)1097-0223(199612)16:13<1237::AID-PD98>3.0.CO;2-T

  19. Biallelic mutations in huntington disease: A new case with just one affected parent, review of the literature and terminology

    American Journal of Medical Genetics Part A

    Volume 167, Issue 5, May 2015, Pages: 1152–1160, Wendy R. Uhlmann, Maria S. Peñaherrera, Wendy P. Robinson, Jeff M. Milunsky, Jane M. Nicholson and Roger L. Albin

    Version of Record online : 3 MAR 2015, DOI: 10.1002/ajmg.a.37009

  20. Molecular detection of new mutations, resolution of ambiguous results and complex genetic counseling issues in Huntington disease

    American Journal of Medical Genetics

    Volume 66, Issue 3, 18 December 1996, Pages: 281–286, R.L. Alford, T. Ashizawa, J. Jankovic, C.T. Caskey and C.S. Richards

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19961218)66:3<281::AID-AJMG9>3.0.CO;2-S