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Journal of Genetic Counseling
|
September 17, 2022
Experiences of receiving an increased chance of sex chromosome aneuploidy result from non-invasive prenatal testing in Australia: "A more complicated scenario than what I had ever realized"
Miranda F Lewit-Mendes, Hazel Robson, Joanne Kelley, et al.
Journal of Community Genetics
|
February 5, 2016
"It gives them more options": preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare
Alison D Archibald, Chriselle L Hickerton, Samantha A Wake, et al.
The Medical Journal of Australia
|
March 4, 2014
Population-based genetic carrier screening for cystic fibrosis in Victoria
Alison D Archibald, John Massie, Melanie J Smith, et al.
European Journal of Human Genetics : EJHG
|
June 21, 2024
Key informant perspectives on implementing genomic newborn screening: a qualitative study guided by the Action, Actor, Context, Target, Time framework
Erin Tutty, Alison D Archibald, Lilian Downie, et al.
European Journal of Human Genetics : EJHG
|
November 2, 2021
Development and use of the Australian reproductive genetic carrier screening decision aid
Emily King, Jane Halliday, Alison D Archibald, et al.
European Journal of Human Genetics : EJHG
|
November 26, 2024
Considering severity in the design of reproductive genetic carrier screening programs: screening for severe conditions
Lucinda Freeman, Alison D Archibald, Lisa Dive, et al.
Australian Journal of General Practice
|
July 1, 2019
Preconception and antenatal carrier screening for genetic conditions: The critical role of general practitioners
Martin B Delatycki, Nigel G Laing, Sarah J Moore, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy
|
October 17, 2012
Development of a fragile X syndrome (FXS) knowledge scale: towards a modified multidimensional measure of informed choice for FXS population carrier screening
Alice G Ames, Alice Jaques, Obioha C Ukoumunne, et al.
Clinical Chemistry
|
July 28, 2025
Assessment of Placental Chromosomal Mosaicism during Prenatal Cell-Free DNA Screening Refines Positive Predictive Values for Fetal Trisomy
Nicola J Flowers, Clare J Love, Katrina L Scarff, et al.
American Journal of Human Genetics
|
May 29, 2025
Public preferences for the value and implementation of genomic newborn screening: Insights from two discrete choice experiments in Australia
Riccarda Peters, Stephanie Best, Fiona Lynch, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 59) with videos related to
Sort By:
Page
of 6
Journal of Genetic Counseling
|
September 17, 2022
Experiences of receiving an increased chance of sex chromosome aneuploidy result from non-invasive prenatal testing in Australia: "A more complicated scenario than what I had ever realized"
Miranda F Lewit-Mendes, Hazel Robson, Joanne Kelley, et al.
Journal of Community Genetics
|
February 5, 2016
"It gives them more options": preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare
Alison D Archibald, Chriselle L Hickerton, Samantha A Wake, et al.
The Medical Journal of Australia
|
March 4, 2014
Population-based genetic carrier screening for cystic fibrosis in Victoria
Alison D Archibald, John Massie, Melanie J Smith, et al.
European Journal of Human Genetics : EJHG
|
June 21, 2024
Key informant perspectives on implementing genomic newborn screening: a qualitative study guided by the Action, Actor, Context, Target, Time framework
Erin Tutty, Alison D Archibald, Lilian Downie, et al.
European Journal of Human Genetics : EJHG
|
November 2, 2021
Development and use of the Australian reproductive genetic carrier screening decision aid
Emily King, Jane Halliday, Alison D Archibald, et al.
European Journal of Human Genetics : EJHG
|
November 26, 2024
Considering severity in the design of reproductive genetic carrier screening programs: screening for severe conditions
Lucinda Freeman, Alison D Archibald, Lisa Dive, et al.
Australian Journal of General Practice
|
July 1, 2019
Preconception and antenatal carrier screening for genetic conditions: The critical role of general practitioners
Martin B Delatycki, Nigel G Laing, Sarah J Moore, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy
|
October 17, 2012
Development of a fragile X syndrome (FXS) knowledge scale: towards a modified multidimensional measure of informed choice for FXS population carrier screening
Alice G Ames, Alice Jaques, Obioha C Ukoumunne, et al.
Clinical Chemistry
|
July 28, 2025
Assessment of Placental Chromosomal Mosaicism during Prenatal Cell-Free DNA Screening Refines Positive Predictive Values for Fetal Trisomy
Nicola J Flowers, Clare J Love, Katrina L Scarff, et al.
American Journal of Human Genetics
|
May 29, 2025
Public preferences for the value and implementation of genomic newborn screening: Insights from two discrete choice experiments in Australia
Riccarda Peters, Stephanie Best, Fiona Lynch, et al.
Page
of 6