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Cancer Cell
|
April 11, 2018
Molecular Signatures of Regression of the Canine Transmissible Venereal Tumor
Dan Frampton, Hagen Schwenzer, Gabriele Marino, et al.
Hereditary Cancer in Clinical Practice
|
April 10, 2021
Impact of national guidelines on use of BRCA1/2 germline testing, risk management advice given to women with pathogenic BRCA1/2 variants and uptake of advice
Bettina Meiser, Rajneesh Kaur, April Morrow, et al.
International Journal of Cardiology
|
February 13, 2021
Investigation of current models of care for genetic heart disease in Australia: A national clinical audit
Rachel Austin, Michael C J Quinn, Clifford Afoakwah, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 1, 2025
Increased yield of genetic diagnoses in inherited heart diseases using expanded genome and RNA-splicing analyses
Yuchen Chang, Emma M Rath, Magdalena Soka, et al.
Cancers
|
October 28, 2023
DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial Glands
Romy Walker, Khalid Mahmood, Julia Como, et al.
Genetics in Medicine Open
|
December 13, 2024
A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship
Rachel Austin, Jaye S Brown, Sarah Casauria, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 13, 2023
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Romy Walker, Khalid Mahmood, Jihoon E Joo, et al.
Journal of Translational Medicine
|
April 26, 2023
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Romy Walker, Khalid Mahmood, Jihoon E Joo, et al.
European Heart Journal
|
August 12, 2025
Titin-related familial dilated cardiomyopathy: factors associated with disease onset
Renee Johnson, Robert A Fletcher, Stacey Peters, et al.
Human Mutation
|
May 28, 2019
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification
Michael T Parsons, Emma Tudini, Hongyan Li, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
Cancer Cell
|
April 11, 2018
Molecular Signatures of Regression of the Canine Transmissible Venereal Tumor
Dan Frampton, Hagen Schwenzer, Gabriele Marino, et al.
Hereditary Cancer in Clinical Practice
|
April 10, 2021
Impact of national guidelines on use of BRCA1/2 germline testing, risk management advice given to women with pathogenic BRCA1/2 variants and uptake of advice
Bettina Meiser, Rajneesh Kaur, April Morrow, et al.
International Journal of Cardiology
|
February 13, 2021
Investigation of current models of care for genetic heart disease in Australia: A national clinical audit
Rachel Austin, Michael C J Quinn, Clifford Afoakwah, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 1, 2025
Increased yield of genetic diagnoses in inherited heart diseases using expanded genome and RNA-splicing analyses
Yuchen Chang, Emma M Rath, Magdalena Soka, et al.
Cancers
|
October 28, 2023
DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial Glands
Romy Walker, Khalid Mahmood, Julia Como, et al.
Genetics in Medicine Open
|
December 13, 2024
A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship
Rachel Austin, Jaye S Brown, Sarah Casauria, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 13, 2023
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Romy Walker, Khalid Mahmood, Jihoon E Joo, et al.
Journal of Translational Medicine
|
April 26, 2023
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Romy Walker, Khalid Mahmood, Jihoon E Joo, et al.
European Heart Journal
|
August 12, 2025
Titin-related familial dilated cardiomyopathy: factors associated with disease onset
Renee Johnson, Robert A Fletcher, Stacey Peters, et al.
Human Mutation
|
May 28, 2019
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification
Michael T Parsons, Emma Tudini, Hongyan Li, et al.
Page
of 2