Pages that link to "Q38221192"

The following pages link to Diagnostic clinical genome and exome sequencing (Q38221192):

Displaying 50 items.

• The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease (Q21819337) (← links)
• Impact of New Genomic Technologies on Understanding Adverse Drug Reactions (Q26787099) (← links)
• Genetic studies of quantitative MCI and AD phenotypes in ADNI: Progress, opportunities, and plans (Q26801647) (← links)
• Clinical application of next-generation sequencing for Mendelian diseases (Q26851246) (← links)
• Perspectives on pharmacogenomics of antiretroviral medications and HIV-associated comorbidities (Q26853274) (← links)
• The diagnostic approach to monogenic very early onset inflammatory bowel disease (Q27015077) (← links)
• "Is It Worth Knowing?" Focus Group Participants' Perceived Utility of Genomic Preconception Carrier Screening (Q27315546) (← links)
• The possibility of clinical sequencing in the management of cancer (Q28072144) (← links)
• Genetics of Tinnitus: An Emerging Area for Molecular Diagnosis and Drug Development (Q28072284) (← links)
• The genetics of premature ovarian failure: current perspectives (Q28084777) (← links)
• Insights from exome sequencing for endocrine disorders (Q28088772) (← links)
• Developing genomic knowledge bases and databases to support clinical management: current perspectives (Q28249073) (← links)
• An eMERGE Clinical Center at Partners Personalized Medicine (Q28601813) (← links)
• Variants of uncertain significance in BRCA: a harbinger of ethical and policy issues to come? (Q30487580) (← links)
• A systematic approach to the reporting of medically relevant findings from whole genome sequencing (Q30622162) (← links)
• Reducing INDEL calling errors in whole genome and exome sequencing data (Q30872081) (← links)
• Precision medicine in the age of big data: The present and future role of large-scale unbiased sequencing in drug discovery and development (Q31017820) (← links)
• Replicate exome-sequencing in a multiple-generation family: improved interpretation of next-generation sequencing data (Q31027821) (← links)
• mirVAFC: A Web Server for Prioritizations of Pathogenic Sequence Variants from Exome Sequencing Data via Classifications. (Q31133404) (← links)
• Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome (Q33421800) (← links)
• High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 Glomerulopathies (Q33425245) (← links)
• DNA Sequence Analysis in Clinical Medicine, Proceeding Cautiously (Q33627712) (← links)
• Insights from early experience of a Rare Disease Genomic Medicine Multidisciplinary Team: a qualitative study (Q33665907) (← links)
• Novel mutations in ADSL for Adenylosuccinate Lyase Deficiency identified by the combination of Trio-WES and constantly updated guidelines (Q33686375) (← links)
• Clinical Applicability of Whole-Exome Sequencing Exemplified by a Study in Young Adults with the Advanced Cryptogenic Cholestatic Liver Diseases. (Q33775587) (← links)
• Clinical sequencing using a next-generation sequencing-based multiplex gene assay in patients with advanced solid tumors. (Q33873653) (← links)
• A taxonomy of medical uncertainties in clinical genome sequencing (Q33918222) (← links)
• Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (Q34526631) (← links)
• Newborn Sequencing in Genomic Medicine and Public Health (Q34549504) (← links)
• Phenotip - a web-based instrument to help diagnosing fetal syndromes antenatally (Q34721140) (← links)
• An approach to pediatric exome and genome sequencing (Q34781498) (← links)
• Living laboratory: whole-genome sequencing as a learning healthcare enterprise (Q34995956) (← links)
• 'Someday it will be the norm': physician perspectives on the utility of genome sequencing for patient care in the MedSeq Project (Q35012563) (← links)
• The fiduciary relationship model for managing clinical genomic "incidental" findings (Q35034175) (← links)
• A one-page summary report of genome sequencing for the healthy adult (Q35143268) (← links)
• Genomic sequencing and the impact of molecular diagnosis on patient care (Q35204406) (← links)
• Oncotator: cancer variant annotation tool (Q35565104) (← links)
• Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic. (Q35648306) (← links)
• Parents are interested in newborn genomic testing during the early postpartum period (Q35674839) (← links)
• Characterizing Participants in the ClinSeq Genome Sequencing Cohort as Early Adopters of a New Health Technology (Q35695017) (← links)
• Management of Incidental Findings in the Era of Next-generation Sequencing (Q35697689) (← links)
• Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings (Q35776062) (← links)
• Use of Targeted Exome Sequencing for Molecular Diagnosis of Skeletal Disorders (Q35779139) (← links)
• Needs Assessment for Research Use of High-Throughput Sequencing at a Large Academic Medical Center (Q35789407) (← links)
• The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists (Q35848496) (← links)
• How to know when physicians are ready for genomic medicine (Q35900275) (← links)
• A Clinical Service to Support the Return of Secondary Genomic Findings in Human Research (Q38635780) (← links)
• Recent developments in dystonia (Q35965335) (← links)
• Molecular heterogeneity in adjacent cells in triple-negative breast cancer (Q35965925) (← links)
• Summarizing polygenic risks for complex diseases in a clinical whole-genome report (Q35990450) (← links)