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Journal of Medical Ethics
|
January 26, 2019
'Is it better not to know certain things?': views of women who have undergone non-invasive prenatal testing on its possible future applications
Hilary Bowman-Smart, Julian Savulescu, Cara Mand, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
January 22, 2013
Current practice and attitudes of Australian obstetricians toward population-based carrier screening for inherited conditions
Zornitza Stark, John Massie, Belinda McClaren, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology
|
February 7, 2019
'Small cost to pay for peace of mind': Women's experiences with non-invasive prenatal testing
Hilary Bowman-Smart, Julian Savulescu, Cara Mand, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 14, 2013
Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research
Liane Ioannou, Belinda J McClaren, John Massie, et al.
Epigenomics
|
November 29, 2021
Sex- and tissue-specific effects of binge-level prenatal alcohol consumption on DNA methylation at birth
Yuk Jing Loke, Evelyne Muggli, Richard Saffery, et al.
Reproductive Biomedicine Online
|
April 24, 2025
Comparing subjective indicators of health in adults aged 27-38 years conceived with and without assisted reproductive technology
Sharon Lewis, Karin Hammarberg, Joanne Kennedy, et al.
Molecular and Biochemical Parasitology
|
September 25, 2002
Leishmania RAB7: characterisation of terminal endocytic stages in an intracellular parasite
Paul W Denny, Sharon Lewis, Jane E Tempero, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 25, 2020
Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing project
Lilian Downie, Jane Halliday, Sharon Lewis, et al.
Journal of Community Genetics
|
July 30, 2013
High school Tay-Sachs disease carrier screening: 5 to 11-year follow-up
Helen Curd, Sharon Lewis, Ivan Macciocca, et al.
Journal of AHIMA
|
May 20, 2014
Managing a patient's right to request restrictions of disclosures to health plans
Barb Beckett, Ben Burton, Kenneth D Clyburn, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 88) with videos related to
Sort By:
Page
of 9
Journal of Medical Ethics
|
January 26, 2019
'Is it better not to know certain things?': views of women who have undergone non-invasive prenatal testing on its possible future applications
Hilary Bowman-Smart, Julian Savulescu, Cara Mand, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
January 22, 2013
Current practice and attitudes of Australian obstetricians toward population-based carrier screening for inherited conditions
Zornitza Stark, John Massie, Belinda McClaren, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology
|
February 7, 2019
'Small cost to pay for peace of mind': Women's experiences with non-invasive prenatal testing
Hilary Bowman-Smart, Julian Savulescu, Cara Mand, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 14, 2013
Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research
Liane Ioannou, Belinda J McClaren, John Massie, et al.
Epigenomics
|
November 29, 2021
Sex- and tissue-specific effects of binge-level prenatal alcohol consumption on DNA methylation at birth
Yuk Jing Loke, Evelyne Muggli, Richard Saffery, et al.
Reproductive Biomedicine Online
|
April 24, 2025
Comparing subjective indicators of health in adults aged 27-38 years conceived with and without assisted reproductive technology
Sharon Lewis, Karin Hammarberg, Joanne Kennedy, et al.
Molecular and Biochemical Parasitology
|
September 25, 2002
Leishmania RAB7: characterisation of terminal endocytic stages in an intracellular parasite
Paul W Denny, Sharon Lewis, Jane E Tempero, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 25, 2020
Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing project
Lilian Downie, Jane Halliday, Sharon Lewis, et al.
Journal of Community Genetics
|
July 30, 2013
High school Tay-Sachs disease carrier screening: 5 to 11-year follow-up
Helen Curd, Sharon Lewis, Ivan Macciocca, et al.
Journal of AHIMA
|
May 20, 2014
Managing a patient's right to request restrictions of disclosures to health plans
Barb Beckett, Ben Burton, Kenneth D Clyburn, et al.
Page
of 9