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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 30, 2018
FMR1 allele size distribution in 35,000 males and females: a comparison of developmental delay and general population cohorts
Claudine M Kraan, Quang M Bui, Mike Field, et al.
European Journal of Human Genetics : EJHG
|
August 22, 2025
Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementation
Michael P Mackley, Pankaj B Agrawal, Sara S Ali, et al.
Oral Oncology
|
February 22, 2021
Relationship of depth of invasion to survival outcomes and patterns of recurrence for T3 oral tongue squamous cell carcinoma
M Newman, P T Dziegielewski, N T A Nguyen, et al.
Pathology
|
May 3, 2025
Guidelines for reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome and spinal muscular atrophy
Edwin Kirk, Linda Mundy, Eric Lee, et al.
BMJ Open
|
June 16, 2026
Developing general practitioner and consumer supports for genomics in Australian primary care: a mixed-methods protocol
Janet C Long, Alison D Archibald, Klay Lamprell, et al.
Nature Medicine
|
October 9, 2025
Feasibility, acceptability and clinical outcomes of the BabyScreen+ genomic newborn screening study
Sebastian Lunke, Lilian Downie, Jade Caruana, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 30, 2017
Informed decision making and psychosocial outcomes in pregnant and nonpregnant women offered population fragile X carrier screening
Sylvia A Metcalfe, Melissa Martyn, Alice Ames, et al.
Journal of Personalized Medicine
|
December 29, 2022
The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation
Alison D Archibald, Belinda J McClaren, Jade Caruana, et al.
Cells
|
September 28, 2023
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on <i>FMR1</i> Premutation
Flora Tassone, Dragana Protic, Emily Graves Allen, et al.
The New England Journal of Medicine
|
November 20, 2024
Nationwide, Couple-Based Genetic Carrier Screening
Edwin P Kirk, Martin B Delatycki, Alison D Archibald, et al.
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of 20
Search research articles
Search
Showing results (181-190 of 191) with videos related to
Sort By:
Page
of 20
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 30, 2018
FMR1 allele size distribution in 35,000 males and females: a comparison of developmental delay and general population cohorts
Claudine M Kraan, Quang M Bui, Mike Field, et al.
European Journal of Human Genetics : EJHG
|
August 22, 2025
Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementation
Michael P Mackley, Pankaj B Agrawal, Sara S Ali, et al.
Oral Oncology
|
February 22, 2021
Relationship of depth of invasion to survival outcomes and patterns of recurrence for T3 oral tongue squamous cell carcinoma
M Newman, P T Dziegielewski, N T A Nguyen, et al.
Pathology
|
May 3, 2025
Guidelines for reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome and spinal muscular atrophy
Edwin Kirk, Linda Mundy, Eric Lee, et al.
BMJ Open
|
June 16, 2026
Developing general practitioner and consumer supports for genomics in Australian primary care: a mixed-methods protocol
Janet C Long, Alison D Archibald, Klay Lamprell, et al.
Nature Medicine
|
October 9, 2025
Feasibility, acceptability and clinical outcomes of the BabyScreen+ genomic newborn screening study
Sebastian Lunke, Lilian Downie, Jade Caruana, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 30, 2017
Informed decision making and psychosocial outcomes in pregnant and nonpregnant women offered population fragile X carrier screening
Sylvia A Metcalfe, Melissa Martyn, Alice Ames, et al.
Journal of Personalized Medicine
|
December 29, 2022
The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation
Alison D Archibald, Belinda J McClaren, Jade Caruana, et al.
Cells
|
September 28, 2023
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on <i>FMR1</i> Premutation
Flora Tassone, Dragana Protic, Emily Graves Allen, et al.
The New England Journal of Medicine
|
November 20, 2024
Nationwide, Couple-Based Genetic Carrier Screening
Edwin P Kirk, Martin B Delatycki, Alison D Archibald, et al.
Page
of 20