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Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 22, 2013
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencingRobert C Green, Jonathan S Berg, Wayne W Grody, et al.
Cardiology and Cardiovascular Medicine|March 30, 2026
Novel Missense Variants in TRIM37 Associated with Mulibrey Nanism and Complex Congenital Heart DiseaseGloria K E Zodanu, Angela C Zeigler, Jordan Mudery, et al.
The Journal of Molecular Diagnostics : JMD|October 13, 2018
Electric Field-Induced Release and Measurement Liquid Biopsy for Noninvasive Early Lung Cancer AssessmentFang Wei, Charles M Strom, Jordan Cheng, et al.
International Journal of Molecular Sciences|May 25, 2024
High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart DefectsGloria K E Zodanu, John H Hwang, Zubin Mehta, et al.
American Journal of Human Genetics|March 3, 2015
De novo nonsense mutations in KAT6A, a lysine acetyl-transferase gene, cause a syndrome including microcephaly and global developmental delayValerie A Arboleda, Hane Lee, Naghmeh Dorrani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 26, 2005
Developing a sustainable process to provide quality control materials for genetic testingBin Chen, Catherine D O' Connell, D Joe Boone, et al.
Academic Pathology|August 18, 2017
The Case for Laboratory Developed Procedures: Quality and Positive Impact on Patient CareKaren L Kaul, Linda M Sabatini, Gregory J Tsongalis, et al.
Archives of Pathology & Laboratory Medicine|August 26, 2014
College of American Pathologists' laboratory standards for next-generation sequencing clinical testsNazneen Aziz, Qin Zhao, Lynn Bry, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2024
Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participantsAmir Hossein Saeidian, Michael E March, Leila Youssefian, et al.
International Journal of Molecular Sciences|March 13, 2025
Whole-Exome Sequencing Identifies Novel GATA5/6 Variants in Right-Sided Congenital Heart DefectsGloria K E Zodanu, John H Hwang, Jordan Mudery, et al.
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