35 results on '"Langlois, Sylvie"'
Search Results
2. Comprehensive Genomic Analysis of Cemento-Ossifying Fibroma
3. Outlier expression of isoforms by targeted or total RNA sequencing identifies clinically significant genomic variants in hematolymphoid tumors
4. Implementation of the BC Congenital Anomalies Surveillance System (BCCASS)
5. Whole-transcriptome analysis in acute lymphoblastic leukemia: a report from the DFCI ALL Consortium Protocol 16-001
6. Current controversy in prenatal diagnosis: The use of cfDNA to screen for monogenic conditions in low risk populations is ready for clinical use.
7. Characterisation of FLT3 alterations in childhood acute lymphoblastic leukaemia
8. Current controversy in prenatal diagnosis: The use of cfDNA to screen for monogenic conditions in low risk populations is ready for clinical use
9. Comprehensive genomic analysis of cemento-ossifying fibroma
10. Genetic counselling considerations with genetic/genomic testing in Neonatal and Pediatric Intensive Care Units: A scoping review.
11. Expansion of non-invasive prenatal screening to the screening of 10 types of chromosomal anomalies: a cost-effectiveness analysis
12. P537: Evaluating parental empowerment and satisfaction in neonatal intensive care units for families experiencing genetic testing: A mixed-methods study
13. Impact of Variation in Practice in the Prenatal Reporting of Variants of Uncertain Significance by Commercial Laboratories: Need for Greater Adherence to Published Guidelines
14. Prenatal screening and diagnosis of sex chromosome conditions: The new normal?
15. The practice of genomic medicine: A delineation of the process and its governing principles
16. Germline Platelet-derived growth factor receptor beta p.R987W pathogenic variant in 2 children with brain tumors
17. Clinical response to dabrafenib and chemotherapy in clonally-related histiocytosis and acute lymphoblastic leukemia
18. Children with Acute Lymphoblastic Leukemia and Early Thrombosis Have Dysregulated Coagulation-Related Genes and Pathways
19. Validation of case definition algorithms for the ascertainment of congenital anomalies
20. Germline PDGFRB p.R987W pathogenic variant in two children with brain tumors
21. Impact of variation in practice in the prenatal reporting of variants of uncertain significance by commercial laboratories: Need for greater adherence to published guidelines
22. Improving Fetal Fraction of Noninvasive Prenatal Screening Samples Collected in EDTA-Gel Tubes Using Gel Size Selection
23. Outlier expression of isoforms by targeted RNA sequencing as clinical markers of genomic variants in B lymphoblastic leukemia and other tumor types
24. Evaluation of out‐of‐pocket pay genetic testing in a publicly funded healthcare system.
25. Real-time molecular classification of leukemias
26. Abstract 3897: Ribosomal translational regulation is a potential mechanism for leukemia-related thrombo-embolic event in childhood acute lymphoblastic leukemia
27. Validation of case definition algorithms for the ascertainment of congenital anomalies.
28. Effect of preexamination conditions in a centralized-testing model of non-invasive prenatal screening
29. Clinical application of fetal genome-wide sequencing during pregnancy: position statement of the Canadian College of Medical Geneticists.
30. Clinical application of fetal genome-wide sequencing during pregnancy: position statement of the Canadian College of Medical Geneticists
31. Effect of preexamination conditions in a centralized-testing model of non-invasive prenatal screening.
32. Out‐of‐pocket and private pay in clinical genetic testing: A scoping review.
33. Current controversies in prenatal diagnosis: Expanded NIPT that includes conditions other than trisomies 13, 18, and 21 should be offered.
34. Response to Wynn and Hokovec Regarding "The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use".
35. Clinical response to dabrafenib and chemotherapy in clonally-related histiocytosis and acute lymphoblastic leukemia.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.