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Cliff Meldrum

Showing results (21-30 of 28) with videos related to

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Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|June 20, 2012
BRCA mutation frequency and patterns of treatment response in BRCA mutation-positive women with ovarian cancer: a report from the Australian Ovarian Cancer Study GroupKathryn Alsop, Sian Fereday, Cliff Meldrum, et al.
Archives of Pathology & Laboratory Medicine|February 16, 2012
Multisite analytic performance studies of a real-time polymerase chain reaction assay for the detection of BRAF V600E mutations in formalin-fixed, paraffin-embedded tissue specimens of malignant melanomaSteven Anderson, Kenneth J Bloom, Dino U Vallera, et al.
Methods and Protocols|July 2, 2021
A Pathway to Precision Medicine for Aboriginal Australians: A Study ProtocolYeu-Yao Cheng, Jack Nunn, John Skinner, et al.
Hereditary Cancer in Clinical Practice|December 31, 2013
The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patientsBente A Talseth-Palmer, Juul T Wijnen, Eva K Andreassen, et al.
Australian Health Review : a Publication of the Australian Hospital Association|October 16, 2023
Making good on the promise of genomics in healthcare: the NSW Health perspectiveDeb Willcox, Ronald J A Trent, Nigel Lyons, et al.
American Journal of Human Genetics|February 7, 2008
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardationGuy Froyen, Mark Corbett, Joke Vandewalle, et al.
Human Mutation|October 29, 2015
Mandibulofacial Dysostosis with Microcephaly: Mutation and Database UpdateLijia Huang, Megan R Vanstone, Taila Hartley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2024
Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohortKerith-Rae Dias, Rupendra Shrestha, Deborah Schofield, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|June 20, 2012
BRCA mutation frequency and patterns of treatment response in BRCA mutation-positive women with ovarian cancer: a report from the Australian Ovarian Cancer Study GroupKathryn Alsop, Sian Fereday, Cliff Meldrum, et al.
Archives of Pathology & Laboratory Medicine|February 16, 2012
Multisite analytic performance studies of a real-time polymerase chain reaction assay for the detection of BRAF V600E mutations in formalin-fixed, paraffin-embedded tissue specimens of malignant melanomaSteven Anderson, Kenneth J Bloom, Dino U Vallera, et al.
Methods and Protocols|July 2, 2021
A Pathway to Precision Medicine for Aboriginal Australians: A Study ProtocolYeu-Yao Cheng, Jack Nunn, John Skinner, et al.
Hereditary Cancer in Clinical Practice|December 31, 2013
The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patientsBente A Talseth-Palmer, Juul T Wijnen, Eva K Andreassen, et al.
Australian Health Review : a Publication of the Australian Hospital Association|October 16, 2023
Making good on the promise of genomics in healthcare: the NSW Health perspectiveDeb Willcox, Ronald J A Trent, Nigel Lyons, et al.
American Journal of Human Genetics|February 7, 2008
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardationGuy Froyen, Mark Corbett, Joke Vandewalle, et al.
Human Mutation|October 29, 2015
Mandibulofacial Dysostosis with Microcephaly: Mutation and Database UpdateLijia Huang, Megan R Vanstone, Taila Hartley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2024
Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohortKerith-Rae Dias, Rupendra Shrestha, Deborah Schofield, et al.
Pageof 3