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Editorial: Educating Health Professionals in Genomic Medicine: Evidence-Based Strategies and Approaches.
- Published in:
- 2020
- By:
- Publication type:
- Editorial
Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census.
- Published in:
- Journal of Genetic Counseling, 2019, v. 28, n. 2, p. 367, doi. 10.1002/jgc4.1101
- By:
- Publication type:
- Article
Personal genomic testing for nutrition and wellness in Australia: A content analysis of online information.
- Published in:
- Nutrition & Dietetics, 2019, v. 76, n. 3, p. 263, doi. 10.1111/1747-0080.12516
- By:
- Publication type:
- Article
'Taking Its Toll': The Challenges of Working in Fetal Medicine.
- Published in:
- Birth: Issues in Perinatal Care, 2013, v. 40, n. 1, p. 52, doi. 10.1111/birt.12029
- By:
- Publication type:
- Article
Human Genetics Society of Australasia Position Statement: Online DNA Testing.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Key informants' perspectives of implementing chromosomal microarrays into clinical practice in australia.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Key Informants’ Perspectives of Implementing Chromosomal Microarrays Into Clinical Practice in Australia.
- Published in:
- Twin Research & Human Genetics, 2013, v. 16, n. 4, p. 833, doi. 10.1017/thg.2013.43
- By:
- Publication type:
- Article
Current Practice and Attitudes of Australian Obstetricians Toward Population-Based Carrier Screening for Inherited Conditions.
- Published in:
- Twin Research & Human Genetics, 2013, v. 16, n. 2, p. 601, doi. 10.1017/thg.2012.152
- By:
- Publication type:
- Article
Impaired response inhibition is associated with self-reported symptoms of depression, anxiety, and ADHD in female FMR1 premutation carriers.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 1, p. 41, doi. 10.1002/ajmg.b.32203
- By:
- Publication type:
- Article
Considerations for Reporting Genome Results to Patients.
- Published in:
- Journal of Paediatrics & Child Health, 2013, v. 49, n. 1, p. 82, doi. 10.1111/jpc.12046
- By:
- Publication type:
- Article
Clinical audit of genetic testing and referral patterns for fragile X and associated conditions.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 6, p. 1439, doi. 10.1002/ajmg.a.37603
- By:
- Publication type:
- Article
'It's about having the choice': Stakeholder perceptions of population-based genetic carrier screening for fragile X syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 1, p. 48, doi. 10.1002/ajmg.a.35674
- By:
- Publication type:
- Article
Investigating genomic medicine practice and perceptions amongst Australian non-genetics physicians to inform education and implementation.
- Published in:
- NPJ Genomic Medicine, 2023, v. 8, n. 1, p. 1, doi. 10.1038/s41525-023-00360-1
- By:
- Publication type:
- Article
The expectations and realities of nutrigenomic testing in australia: A qualitative study.
- Published in:
- Health Expectations, 2021, v. 24, n. 2, p. 670, doi. 10.1111/hex.13216
- By:
- Publication type:
- Article
Development of a fragile X syndrome ( FXS) knowledge scale: towards a modified multidimensional measure of informed choice for FXS population carrier screening.
- Published in:
- Health Expectations, 2015, v. 18, n. 1, p. 69, doi. 10.1111/hex.12009
- By:
- Publication type:
- Article
A mixed methods study of age at diagnosis and diagnostic odyssey for Duchenne muscular dystrophy.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 10, p. 1294, doi. 10.1038/ejhg.2014.301
- By:
- Publication type:
- Article
A mixed methods exploration of families' experiences of the diagnosis of childhood spinal muscular atrophy.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 5, p. 575, doi. 10.1038/ejhg.2014.147
- By:
- Publication type:
- Article
Measuring informed choice in population-based reproductive genetic screening: a systematic review.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 1, p. 8, doi. 10.1038/ejhg.2014.89
- By:
- Publication type:
- Article
Availability of treatment drives decisions of genetic health professionals about disclosure of incidental findings.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 10, p. 1225, doi. 10.1038/ejhg.2014.11
- By:
- Publication type:
- Article
A qualitative exploration of mothers' and fathers' experiences of having a child with Klinefelter syndrome and the process of reaching this diagnosis.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 1, p. 18, doi. 10.1038/ejhg.2013.102
- By:
- Publication type:
- Article
An exploration of genetic health professionals' experience with direct-to-consumer genetic testing in their clinical practice.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 8, p. 825, doi. 10.1038/ejhg.2012.13
- By:
- Publication type:
- Article
ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 5, p. 505, doi. 10.1038/ejhg.2011.247
- By:
- Publication type:
- Article
Uptake of carrier testing in families after cystic fibrosis diagnosis through newborn screening.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 10, p. 1084, doi. 10.1038/ejhg.2010.78
- By:
- Publication type:
- Article
Carrier screening for Beta-thalassaemia: a review of international practice.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 10, p. 1077, doi. 10.1038/ejhg.2010.90
- By:
- Publication type:
- Article
‘It is not in my world’: an exploration of attitudes and influences associated with cystic fibrosis carrier screening.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 435, doi. 10.1038/sj.ejhg.5201965
- By:
- Publication type:
- Article
It's ‘back to school’ for genetic screening.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 4, p. 384, doi. 10.1038/sj.ejhg.5201581
- By:
- Publication type:
- Article
Preparing Medical Specialists for Genomic Medicine: Continuing Education Should Include Opportunities for Experiential Learning.
- Published in:
- Frontiers in Genetics, 2020, p. 1, doi. 10.3389/fgene.2020.00151
- By:
- Publication type:
- Article
Development of an Evidence-Based, Theory-Informed National Survey of Physician Preparedness for Genomic Medicine and Preferences for Genomics Continuing Education.
- Published in:
- Frontiers in Genetics, 2020, p. 1, doi. 10.3389/fgene.2020.00059
- By:
- Publication type:
- Article
Ensuring Best Practice in Genomic Education and Evaluation: A Program Logic Approach.
- Published in:
- Frontiers in Genetics, 2019, v. 10, p. 1, doi. 10.3389/fgene.2019.01057
- By:
- Publication type:
- Article
Preparing Medical Specialists to Practice Genomic Medicine: Education an Essential Part of a Broader Strategy.
- Published in:
- Frontiers in Genetics, 2019, p. 1, doi. 10.3389/fgene.2019.00789
- By:
- Publication type:
- Article
Disclosing Genetic Research Results After Death of Pediatric Patients.
- Published in:
- JAMA: Journal of the American Medical Association, 2008, v. 300, n. 14, p. 1693, doi. 10.1001/jama.300.14.1693
- By:
- Publication type:
- Article
A Long-term Outcome Study of Intersex Conditions.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2005, v. 18, n. 6, p. 555, doi. 10.1515/jpem.2005.18.6.555
- By:
- Publication type:
- Article
'It's Challenging on a Personal Level'-Exploring the 'Lived Experience' of Australian and Canadian Prenatal Genetic Counselors.
- Published in:
- Journal of Genetic Counseling, 2010, v. 19, n. 6, p. 640, doi. 10.1007/s10897-010-9315-z
- By:
- Publication type:
- Article
“Testing Times, Challenging Choices”: An Australian Study of Prenatal Genetic Counseling.
- Published in:
- Journal of Genetic Counseling, 2010, v. 19, n. 1, p. 22, doi. 10.1007/s10897-009-9248-6
- By:
- Publication type:
- Article
The Importance of Program Evaluation: How Can it be Applied to Diverse Genetics Education Settings?
- Published in:
- Journal of Genetic Counseling, 2008, v. 17, n. 2, p. 170, doi. 10.1007/s10897-007-9138-8
- By:
- Publication type:
- Article
A case for cystic fibrosis carrier testing in the general population.
- Published in:
- 2011
- By:
- Publication type:
- Letter
In vitro responses of human prostate tumour cell lines to a range of antitumour agents.
- Published in:
- International Journal of Cancer, 1983, v. 32, n. 3, p. 351, doi. 10.1002/ijc.2910320315
- By:
- Publication type:
- Article
Auditing the use of genetics educational technologies in Australian secondary schools.
- Published in:
- Teaching Science: The Journal of the Australian Science Teachers Association, 2007, v. 53, n. 4, p. 36
- By:
- Publication type:
- Article
Evaluation of a decision aid for prenatal testing of fetal abnormalities: a cluster randomised trial [ISRCTN22532458].
- Published in:
- BMC Public Health, 2006, v. 6, n. 1, p. 96, doi. 10.1186/1471-2458-6-96
- By:
- Publication type:
- Article
Prenatal β-thalassemia carrier screening in Australia: healthcare professionals' perspectives of clinical practice.
- Published in:
- Prenatal Diagnosis, 2014, v. 34, n. 3, p. 246, doi. 10.1002/pd.4297
- By:
- Publication type:
- Article
Prenatal [beta]-thalassemia carrier screening in Australia: healthcare professionals' perspectives of clinical practice.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Educating general practitioners about prenatal testing: approaches and challenges.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 7, p. 592, doi. 10.1002/pd.1202
- By:
- Publication type:
- Article
General practitioners' views on genomics, practice and education: A qualitative interview study.
- Published in:
- Australian Journal of General Practice, 2021, v. 50, n. 10, p. 747, doi. 10.31128/ajgp-05-20-5448
- By:
- Publication type:
- Article
Experiences of prenatal diagnosis and decision-making about termination of pregnancy: A qualitative study.
- Published in:
- Australian & New Zealand Journal of Obstetrics & Gynaecology, 2016, v. 56, n. 6, p. 605, doi. 10.1111/ajo.12501
- By:
- Publication type:
- Article
Improving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention.
- Published in:
- BMC Medical Genetics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2350-15-33
- By:
- Publication type:
- Article