Quest Diagnostics Manuals & User Guides

Quest Diagnostics Quanum Practice Solutionsi kasutusjuhend

23. juuli 2023

Quanum ® praktikalahenduste pakkumise lõpetamine Kliendi KKK – juuli 2023 Quanum Practice Solutionsi katkestamine Millised on patsiendiandmete toomise või neile juurdepääsu võimalused? Valik Tulemus Andmete ekstraheerimise eksport Näitample use case Provider wants to take the most data possible…

Brand: Quest Diagnostics

Quest Diagnostics päriliku trombofiilia geneetilise ülevaate testi kasutusjuhend

15. juuli 2023

Genetic Insights: quick reference guide for healthcare providers This guide is intended to facilitate discussion between a provider and their patient. Genetic Insights test results: Hereditary thrombophilia Key results The DNA variant c.*97G>A associated with hereditary thrombophilia was found in…

Brand: Quest Diagnostics

Quest Diagnostics Lynchi sündroomi geneetilise ülevaate testi kasutusjuhend

15. juuli 2023

Quest Diagnostics Lynch Syndrome Genetic Insights Test User Guide Key results A pathogenic or likely pathogenic variant associated with Lynch syndrome was found in the MSH2 gene. People with Lynch syndrome have a significantly increased risk of developing certain cancers,…

Brand: Quest Diagnostics

Quest Diagnostics PALB2 seotud päriliku vähi kasutusjuhend

15. juuli 2023

Genetic Insights: quick reference guide for healthcare providers This guide is intended to facilitate a discussion between a provider and their patient. Genetic Insights test results: PALB2-associated hereditary cancer Key results A DNA variant associated with an increased risk of…

Brand: Quest Diagnostics

Quest Diagnostics päriliku trombofiilia kasutusjuhend

15. juuli 2023

Genetic Insights: quick reference guide for healthcare providers This guide is intended to facilitate discussion between a provider and their patient. Genetic Insights test results: Hereditary thrombophilia Key results The DNA variant c.*97G>A was found in the F2 gene and…

Brand: Quest Diagnostics

Quest Diagnostics Lynchi sündroomi kasutusjuhend

15. juuli 2023

Quest Diagnostics Lynch Syndrome Key Results A pathogenic or likely pathogenic variant associated with Lynch syndrome was found in the PMS2 gene. People with Lynch syndrome have a significantly increased risk of developing certain cancers, especially colon cancer and uterine…

Brand: Quest Diagnostics

Quest Diagnostics CHEK2 seotud päriliku vähi kasutusjuhend

15. juuli 2023

Genetic Insights: quick reference guide for healthcare providers This guide is intended to facilitate a discussion between a provider and their patient. Genetic Insights test results: CHEK2-associated hereditary cancer Key results A variant called c.470T>C (p.Ile157Thr) was found in the…

Brand: Quest Diagnostics

Quest Diagnostics Genetic Insights Testi kasutusjuhend

15. juuli 2023

Genetic Insights: quick reference guide for healthcare providers This guide is intended to facilitate a discussion between a provider and their patient. Genetic Insights test results: Classical Ehlers-Danlos syndrome Key results A variant called c.470T>C (p.Ile157Thr) was found in the…

Brand: Quest Diagnostics

Quest Diagnostics Genetic Insights Testi kasutusjuhend

15. juuli 2023

Genetic Insights: quick reference guide for healthcare providers This guide is intended to facilitate a discussion between a provider and their patient. Genetic Insights test results: Cystic fibrosis Key results Two different pathogenic or likely pathogenic variants associated with having…

Brand: Quest Diagnostics

Quest Diagnostics CHEK2 Genetic Insights Testi kasutusjuhend

15. juuli 2023

Quest Diagnostics CHEK2 Genetic Insights Test Key results A variant was found in the CHEK2 gene that is associated with an increased risk of breast cancer in females, prostate cancer in males, colon cancer, and possibly certain other cancers. Next…

Brand: Quest Diagnostics