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Clinical Endocrinology
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September 16, 2021
A practical guide to genetic testing in endocrinology
Louise Izatt, Martina M Owens, Heather Pierce, et al.
Genome Medicine
|
July 22, 2022
Assessing the clinical utility of protein structural analysis in genomic variant classification: experiences from a diagnostic laboratory
Richard C Caswell, Adam C Gunning, Martina M Owens, et al.
Journal of the Endocrine Society
|
November 19, 2019
Using Structural Analysis <i>In Silico</i> to Assess the Impact of Missense Variants in MEN1
Richard C Caswell, Martina M Owens, Adam C Gunning, et al.
Scientific Reports
|
February 18, 2016
Pitfalls of haplotype phasing from amplicon-based long-read sequencing
Thomas W Laver, Richard C Caswell, Karen A Moore, et al.
JAMA Network Open
|
June 27, 2025
Medullary Thyroid Cancer Risk and Mortality in Carriers of Incidentally Identified MEN2A RET Variants
Courtney E West, Uyenlinh L Mirshahi, Katherine S Ruth, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B
|
November 7, 2013
A comparison of methods for EGFR mutation testing in non-small cell lung cancer
Elizabeth C Young, Martina M Owens, Idowu Adebiyi, et al.
American Journal of Human Genetics
|
July 8, 2017
WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features
Cara M Skraban, Constance F Wells, Preetha Markose, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Clinical Endocrinology
|
September 16, 2021
A practical guide to genetic testing in endocrinology
Louise Izatt, Martina M Owens, Heather Pierce, et al.
Genome Medicine
|
July 22, 2022
Assessing the clinical utility of protein structural analysis in genomic variant classification: experiences from a diagnostic laboratory
Richard C Caswell, Adam C Gunning, Martina M Owens, et al.
Journal of the Endocrine Society
|
November 19, 2019
Using Structural Analysis <i>In Silico</i> to Assess the Impact of Missense Variants in MEN1
Richard C Caswell, Martina M Owens, Adam C Gunning, et al.
Scientific Reports
|
February 18, 2016
Pitfalls of haplotype phasing from amplicon-based long-read sequencing
Thomas W Laver, Richard C Caswell, Karen A Moore, et al.
JAMA Network Open
|
June 27, 2025
Medullary Thyroid Cancer Risk and Mortality in Carriers of Incidentally Identified MEN2A RET Variants
Courtney E West, Uyenlinh L Mirshahi, Katherine S Ruth, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B
|
November 7, 2013
A comparison of methods for EGFR mutation testing in non-small cell lung cancer
Elizabeth C Young, Martina M Owens, Idowu Adebiyi, et al.
American Journal of Human Genetics
|
July 8, 2017
WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features
Cara M Skraban, Constance F Wells, Preetha Markose, et al.
Page
of 1