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Wellcome Open Research
|
November 6, 2023
Public engagement with genomics
Anna Middleton, Avery Adams, Hugbaad Aidid, et al.
Respirology (Carlton, Vic.)
|
April 19, 2016
Physiotherapy for cystic fibrosis in Australia and New Zealand: A clinical practice guideline
Brenda M Button, Christine Wilson, Ruth Dentice, et al.
Lancet (London, England)
|
December 23, 2014
Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data
Caroline F Wright, Tomas W Fitzgerald, Wendy D Jones, et al.
European Journal of Human Genetics : EJHG
|
October 7, 2018
The Global State of the Genetic Counseling Profession
MaryAnn Abacan, Lamia Alsubaie, Kristine Barlow-Stewart, et al.
American Journal of Human Genetics
|
September 18, 2020
Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?
Anna Middleton, Richard Milne, Mohamed A Almarri, et al.
Genome Medicine
|
May 26, 2021
Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries
Richard Milne, Katherine I Morley, Mohamed A Almarri, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
December 21, 2023
Standards for the care of people with cystic fibrosis; establishing and maintaining health
Kevin W Southern, Charlotte Addy, Scott C Bell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 7, 2022
Return of genomic results does not motivate intent to participate in research for all: Perspectives across 22 countries
Richard Milne, Katherine I Morley, Mohamed A Almarri, et al.
Cell Genomics
|
January 24, 2022
GA4GH: International policies and standards for data sharing across genomic research and healthcare
Heidi L Rehm, Angela J H Page, Lindsay Smith, et al.
Page
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Search research articles
Search
Showing results (91-100 of 99) with videos related to
Sort By:
Page
of 10
You have reached the last page of results.
This site can display upto 99 results.
Wellcome Open Research
|
November 6, 2023
Public engagement with genomics
Anna Middleton, Avery Adams, Hugbaad Aidid, et al.
Respirology (Carlton, Vic.)
|
April 19, 2016
Physiotherapy for cystic fibrosis in Australia and New Zealand: A clinical practice guideline
Brenda M Button, Christine Wilson, Ruth Dentice, et al.
Lancet (London, England)
|
December 23, 2014
Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data
Caroline F Wright, Tomas W Fitzgerald, Wendy D Jones, et al.
European Journal of Human Genetics : EJHG
|
October 7, 2018
The Global State of the Genetic Counseling Profession
MaryAnn Abacan, Lamia Alsubaie, Kristine Barlow-Stewart, et al.
American Journal of Human Genetics
|
September 18, 2020
Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?
Anna Middleton, Richard Milne, Mohamed A Almarri, et al.
Genome Medicine
|
May 26, 2021
Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries
Richard Milne, Katherine I Morley, Mohamed A Almarri, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
December 21, 2023
Standards for the care of people with cystic fibrosis; establishing and maintaining health
Kevin W Southern, Charlotte Addy, Scott C Bell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 7, 2022
Return of genomic results does not motivate intent to participate in research for all: Perspectives across 22 countries
Richard Milne, Katherine I Morley, Mohamed A Almarri, et al.
Cell Genomics
|
January 24, 2022
GA4GH: International policies and standards for data sharing across genomic research and healthcare
Heidi L Rehm, Angela J H Page, Lindsay Smith, et al.
Page
of 10