32 results on '"Delatycki, Martin B."'
Search Results
2. Views of healthcare professionals on the inclusion of genes associated with non-syndromic hearing loss in reproductive genetic carrier screening
3. Health professionals’ views and experiences of the Australian moratorium on genetic testing and life insurance: A qualitative study
4. Unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencing
5. Gene selection for the Australian Reproductive Genetic Carrier Screening Project (“Mackenzie’s Mission”)
6. Genetic discrimination by Australian insurance companies: a survey of consumer experiences
7. A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis
8. Correction: Community concerns about genetic discrimination in life insurance persist in Australia: A survey of consumers offered genetic testing
9. Community concerns about genetic discrimination in life insurance persist in Australia: A survey of consumers offered genetic testing
10. Correction to: Genetic discrimination by Australian insurance companies: a survey of consumer experiences
11. Unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencing
12. Expanded reproductive carrier screening—how can we do the most good and cause the least harm?
13. Gene selection for the Australian Reproductive Genetic Carrier Screening Project (“Mackenzie’s Mission”)
14. Correction to: Genetic discrimination by Australian insurance companies: a survey of consumer experiences
15. Genetic discrimination by Australian insurance companies: a survey of consumer experiences
16. Presymptomatic testing of those at 25% risk of autosomal dominant neurodegenerative disease- testing team beware
17. Outcomes of a randomised controlled trial of a complex genetic counselling intervention to improve family communication
18. Attitudes and opinions of pregnant women who are not offered cystic fibrosis carrier screening
19. Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome
20. ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible
21. Carrier screening for Beta-thalassaemia: a review of international practice
22. Listen carefully: LIS1 and DCX MLPA in lissencephaly and subcortical band heterotopia
23. Problems assessing uptake of Huntington disease predictive testing and a proposed solution
24. Health first, genetics second: exploring families' experiences of communicating genetic information
25. ‘It is not in my world’: an exploration of attitudes and influences associated with cystic fibrosis carrier screening
26. Communicating genetic information in families – a review of guidelines and position papers
27. Attitudes and opinions of pregnant women who are not offered cystic fibrosis carrier screening.
28. Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome.
29. Problems assessing uptake of Huntington disease predictive testing and a proposed solution.
30. ‘It is not in my world’: an exploration of attitudes and influences associated with cystic fibrosis carrier screening.
31. It's ‘back to school’ for genetic screening.
32. Listen carefully: LIS1 and DCX MLPA in lissencephaly and subcortical band heterotopia.
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