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There are 19770 results for: content related to: Evaluation of a multi-disease carrier screening programme in Ashkenazi Jewish high schools

  1. Prenatal and preconception population carrier screening for cystic fibrosis in Australia: Where are we up to?

    Australian and New Zealand Journal of Obstetrics and Gynaecology

    Volume 54, Issue 6, December 2014, Pages: 503–509, John Massie, Liane Ioannou and Martin Delatycki

    Version of Record online : 28 OCT 2014, DOI: 10.1111/ajo.12255

  2. Implementation of ironXS: a study of the acceptability and feasibility of genetic screening for hereditary hemochromatosis in high schools

    Clinical Genetics

    Volume 77, Issue 3, March 2010, Pages: 241–248, MB Delatycki, M Wolthuizen, V Collins, E Varley, J Craven, KJ Allen, MA Aitken, L Bond, PJ Lockhart, GR Wilson, I Macciocca and SA Metcalfe

    Version of Record online : 23 NOV 2009, DOI: 10.1111/j.1399-0004.2009.01308.x

  3. Family Relations in the Genomic Era: Communicating about Intergenerational Transmission of Risk for Disability

    Family Relations

    Volume 63, Issue 1, February 2014, Pages: 85–100, Donald B. Bailey, Megan A. Lewis, Myra Roche and Cynthia M. Powell

    Version of Record online : 11 JAN 2014, DOI: 10.1111/fare.12054

  4. Prenatal β-thalassemia carrier screening in Australia: healthcare professionals' perspectives of clinical practice

    Prenatal Diagnosis

    Volume 34, Issue 3, March 2014, Pages: 246–250, Nicole E. Cousens, Clara L. Gaff, Martin B. Delatycki and Sylvia A. Metcalfe

    Version of Record online : 19 JAN 2014, DOI: 10.1002/pd.4297

  5. Heterozygote Carrier Testing in High Schools Abroad: What are the Lessons for the U.S.?

    The Journal of Law, Medicine & Ethics

    Volume 34, Issue 4, Winter 2006, Pages: 753–764, Lainie Friedman Ross

    Version of Record online : 23 NOV 2006, DOI: 10.1111/j.1748-720X.2006.00096.x

  6. Ashkenazi Jewish population screening for Tay–Sachs disease: The International and Australian experience

    Journal of Paediatrics and Child Health

    Volume 51, Issue 3, March 2015, Pages: 271–279, Raelia M Lew, Leslie Burnett, Anné L Proos, Kristine Barlow-Stewart, Martin B Delatycki, Agnes Bankier, Harry Aizenberg, Michael J Field, Yemima Berman, Ronald Fleischer and Michael Fietz

    Version of Record online : 13 JUN 2014, DOI: 10.1111/jpc.12632

  7. Informing policy for the Australian context – Costs, outcomes and cost savings of prenatal carrier screening for cystic fibrosis

    Australian and New Zealand Journal of Obstetrics and Gynaecology

    Volume 50, Issue 1, February 2010, Pages: 51–59, Susannah MAXWELL, Kate BRAMELD, Leanne YOUNGS, Elizabeth GEELHOED and Peter O’LEARY

    Version of Record online : 11 FEB 2010, DOI: 10.1111/j.1479-828X.2009.01111.x

  8. “It's something I need to consider”: Decisions about carrier screening for fragile X syndrome in a population of non-pregnant women

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 12, December 2009, Pages: 2731–2738, Alison D. Archibald, Alice M. Jaques, Samantha Wake, Veronica R. Collins, Jonathan Cohen and Sylvia A. Metcalfe

    Version of Record online : 24 NOV 2009, DOI: 10.1002/ajmg.a.33122

  9. Population-based carrier screening for cystic fibrosis in Victoria: The first three years experience

    Australian and New Zealand Journal of Obstetrics and Gynaecology

    Volume 49, Issue 5, October 2009, Pages: 484–489, John MASSIE, Vicki PETROU, Robyn FORBES, Lisette CURNOW, Liane IOANNOU, Desiree DUSART, Agnes BANKIER and Martin DELATYCKI

    Version of Record online : 19 AUG 2009, DOI: 10.1111/j.1479-828X.2009.01045.x

  10. “I'm Healthy, It's Not Going To Be Me”: Exploring experiences of carriers identified through a population reproductive genetic carrier screening panel in Australia

    American Journal of Medical Genetics Part A

    Volume 170, Issue 8, August 2016, Pages: 2052–2059, Catherine A. Beard, David J. Amor, Louisa Di Pietro and Alison D. Archibald

    Version of Record online : 6 MAY 2016, DOI: 10.1002/ajmg.a.37697

  11. HFE p.C282Y heterozygosity is associated with earlier disease onset in Friedreich ataxia

    Movement Disorders

    Volume 29, Issue 7, June 2014, Pages: 940–943, Martin B. Delatycki, Geneieve Tai, Louise Corben, Eppie M. Yiu, Marguerite V. Evans-Galea, Sarah E.M. Stephenson, Lyle Gurrin, Katrina J. Allen, David Lynch and Paul J. Lockhart

    Version of Record online : 3 JAN 2014, DOI: 10.1002/mds.25795

  12. Genetic screening for reproductive purposes at school: Is it a good strategy?

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 2, 15 January 2008, Pages: 264–269, Ayala Frumkin and Joël Zlotogora

    Version of Record online : 13 DEC 2007, DOI: 10.1002/ajmg.a.32069

  13. “It's about having the choice”: Stakeholder perceptions of population-based genetic carrier screening for fragile X syndrome

    American Journal of Medical Genetics Part A

    Volume 161, Issue 1, January 2013, Pages: 48–58, Alison D. Archibald, Chriselle L. Hickerton, Alice M. Jaques, Samantha Wake, Jonathan Cohen and Prof. Sylvia A. Metcalfe

    Version of Record online : 13 DEC 2012, DOI: 10.1002/ajmg.a.35674

  14. “You're one of us now”: Young people describe their experiences of predictive genetic testing for Huntington disease (HD) and familial adenomatous polyposis (FAP)

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 148C, Issue 1, 15 February 2008, Pages: 47–55, Rony E. Duncan, Lynn Gillam, Julian Savulescu, Robert Williamson, John G. Rogers and Martin B. Delatycki

    Version of Record online : 11 JAN 2008, DOI: 10.1002/ajmg.c.30158

  15. Evaluation of a Tay-Sachs Disease screening program

    Clinical Genetics

    Volume 63, Issue 5, May 2003, Pages: 386–392, AA Gason, E Sheffield, A Bankier, MA Aitken, S Metcalfe, K Barlow Stewart and MB Delatycki

    Version of Record online : 7 MAY 2003, DOI: 10.1034/j.1399-0004.2003.00074.x

  16. Population Carrier Screening: Psychological Impact

    Standard Article

    eLS

    Alison D Archibald and Benjamin S Wilfond

    Published Online : 15 JUL 2011, DOI: 10.1002/9780470015902.a0005641.pub2

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    Clinical features of Friedreich's ataxia: classical and atypical phenotypes

    Journal of Neurochemistry

    Volume 126, Issue s1, August 2013, Pages: 103–117, Michael H. Parkinson, Sylvia Boesch, Wolfgang Nachbauer, Caterina Mariotti and Paola Giunti

    Version of Record online : 17 JUL 2013, DOI: 10.1111/jnc.12317

  18. “Holding your breath”: Interviews with young people who have undergone predictive genetic testing for Huntington disease

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 17, 1 September 2007, Pages: 1984–1989, Rony E. Duncan, Lynn Gillam, Julian Savulescu, Robert Williamson, John G. Rogers and Martin B. Delatycki

    Version of Record online : 30 JUL 2007, DOI: 10.1002/ajmg.a.31720

  19. Carrier Screening of Adolescents in Montreal

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    eLS

    Charles R Scriver and John J Mitchell

    Published Online : 15 DEC 2009, DOI: 10.1002/9780470015902.a0005646.pub2

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    Nationwide genetic analysis for molecularly unresolved cystic fibrosis patients in a multiethnic society: implications for preconception carrier screening

    Molecular Genetics & Genomic Medicine

    Volume 5, Issue 3, May 2017, Pages: 223–236, Doron M. Behar, Ori Inbar, Michal Shteinberg, Michal Gur, Huda Mussaffi, David Shoseyov, Moshe Ashkenazi, Soliman Alkrinawi, Concetta Bormans, Fahed Hakim, Meir Mei-Zahav, Malena Cohen-Cymberknoh, Adi Dagan, Dario Prais, Ifat Sarouk, Patrick Stafler, Bat El Bar Aluma, Gidon Akler, Elie Picard, Micha Aviram, Ori Efrati, Galit Livnat, Joseph Rivlin, Lea Bentur, Hannah Blau, Eitan Kerem and Amihood Singer

    Version of Record online : 19 FEB 2017, DOI: 10.1002/mgg3.278