Pages that link to "Q42399564"

The following pages link to Natasha T Strande (Q42399564):

Displaying 23 items.

• Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium (Q28601251) (← links)
• Nonhomologous end joining: a good solution for bad ends (Q33625010) (← links)
• Requirements for 5'dRP/AP lyase activity in Ku. (Q34248869) (← links)
• Organization and dynamics of the nonhomologous end-joining machinery during DNA double-strand break repair (Q35644654) (← links)
• A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing (Q36578258) (← links)
• A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation. (Q37377663) (← links)
• Resolution of complex ends by Nonhomologous end joining - better to be lucky than good? (Q38070431) (← links)
• Defining the Clinical Value of a Genomic Diagnosis in the Era of Next-Generation Sequencing. (Q38846804) (← links)
• Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium (Q42399548) (← links)
• The fidelity of the ligation step determines how ends are resolved during nonhomologous end joining. (Q42744119) (← links)
• Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource (Q44763269) (← links)
• UV sensitive mutations in histone H3 in Saccharomyces cerevisiae that alter specific K79 methylation states genetically act through distinct DNA repair pathways (Q46713104) (← links)
• Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges (Q47131952) (← links)
• Diagnostic utility of exome sequencing in the evaluation of neuromuscular disorders. (Q50127011) (← links)
• The phenotype of multiple congenital anomalies-hypotonia-seizures syndrome 1: report and review. (Q55060248) (← links)
• "Possibly positive or certainly uncertain?": participants' responses to uncertain diagnostic results from exome sequencing. (Q55089341) (← links)
• Combination of exome sequencing and immune testing confirms Aicardi-Goutières syndrome type 5 in a challenging pediatric neurology case (Q57054043) (← links)
• Approaches to carrier testing and results disclosure in translational genomics research: The clinical sequencing exploratory research consortium experience (Q57168322) (← links)
• Navigating the nuances of clinical sequence variant interpretation in Mendelian disease (Q57210317) (← links)
• ClinGen Allele Registry links information about genetic variants (Q57455591) (← links)
• Increasing the diagnostic yield of exome sequencing by copy number variant analysis (Q60301732) (← links)
• Evaluating the clinical validity of gene-disease associations: an evidence-based framework developed by the Clinical Genome Resource (Q61719281) (← links)
• Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients (Q102049373) (← links)