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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 2, 2024
A systematic review and pooled analysis of penetrance estimates of copy-number variants associated with neurodevelopment
Shuxiang Goh, Lavvina Thiyagarajan, Tracy Dudding-Byth, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 6, 2022
The views of people with a lived experience of deafness and the general public regarding genetic testing for deafness in the reproductive setting: A systematic review
Lucinda Freeman, Sarah Righetti, Martin B Delatycki, et al.
European Journal of Human Genetics : EJHG
|
February 9, 2023
Views of healthcare professionals on the inclusion of genes associated with non-syndromic hearing loss in reproductive genetic carrier screening
Lucinda Freeman, Martin B Delatycki, Jackie Leach Scully, et al.
Journal of Genetic Counseling
|
August 3, 2023
Should genes for non-syndromic hearing loss be included in reproductive genetic carrier screening: Views of people with a personal or family experience of deafness
Lucinda Freeman, Lisa Bristowe, Edwin P Kirk, et al.
European Journal of Medical Genetics
|
May 16, 2019
Personal genomic screening: How best to facilitate preparedness of future clients
Jane Fleming, Bronwyn Terrill, Marie Dziadek, et al.
American Journal of Medical Genetics. Part A
|
September 17, 2004
Diagnosis of Proteus syndrome was correct
Edwin P Kirk, Janine M Smith, Michael Field, et al.
European Journal of Human Genetics : EJHG
|
February 25, 2026
Individuals' preferences for future biological sample and genomic data sharing in the Australian Reproductive Genetic Carrier Screening Project
Matilda A Haas, Evanthia O Madelli, Martin B Delatycki, et al.
The Medical Journal of Australia
|
August 7, 2012
Congenital heart disease: current knowledge about causes and inheritance
Gillian M Blue, Edwin P Kirk, Gary F Sholler, et al.
International Journal of Cardiology
|
December 3, 2014
Genetic counselling in parents of children with congenital heart disease significantly improves knowledge about causation and enhances psychosocial functioning
Gillian M Blue, Nadine A Kasparian, Gary F Sholler, et al.
The Medical Journal of Australia
|
February 9, 2011
Salicylate intoxication from teething gel in infancy
Gary D Williams, Edwin P Kirk, Callum J Wilson, et al.
Page
of 12
Search research articles
Search
Showing results (21-30 of 117) with videos related to
Sort By:
Page
of 12
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 2, 2024
A systematic review and pooled analysis of penetrance estimates of copy-number variants associated with neurodevelopment
Shuxiang Goh, Lavvina Thiyagarajan, Tracy Dudding-Byth, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 6, 2022
The views of people with a lived experience of deafness and the general public regarding genetic testing for deafness in the reproductive setting: A systematic review
Lucinda Freeman, Sarah Righetti, Martin B Delatycki, et al.
European Journal of Human Genetics : EJHG
|
February 9, 2023
Views of healthcare professionals on the inclusion of genes associated with non-syndromic hearing loss in reproductive genetic carrier screening
Lucinda Freeman, Martin B Delatycki, Jackie Leach Scully, et al.
Journal of Genetic Counseling
|
August 3, 2023
Should genes for non-syndromic hearing loss be included in reproductive genetic carrier screening: Views of people with a personal or family experience of deafness
Lucinda Freeman, Lisa Bristowe, Edwin P Kirk, et al.
European Journal of Medical Genetics
|
May 16, 2019
Personal genomic screening: How best to facilitate preparedness of future clients
Jane Fleming, Bronwyn Terrill, Marie Dziadek, et al.
American Journal of Medical Genetics. Part A
|
September 17, 2004
Diagnosis of Proteus syndrome was correct
Edwin P Kirk, Janine M Smith, Michael Field, et al.
European Journal of Human Genetics : EJHG
|
February 25, 2026
Individuals' preferences for future biological sample and genomic data sharing in the Australian Reproductive Genetic Carrier Screening Project
Matilda A Haas, Evanthia O Madelli, Martin B Delatycki, et al.
The Medical Journal of Australia
|
August 7, 2012
Congenital heart disease: current knowledge about causes and inheritance
Gillian M Blue, Edwin P Kirk, Gary F Sholler, et al.
International Journal of Cardiology
|
December 3, 2014
Genetic counselling in parents of children with congenital heart disease significantly improves knowledge about causation and enhances psychosocial functioning
Gillian M Blue, Nadine A Kasparian, Gary F Sholler, et al.
The Medical Journal of Australia
|
February 9, 2011
Salicylate intoxication from teething gel in infancy
Gary D Williams, Edwin P Kirk, Callum J Wilson, et al.
Page
of 12