| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Chromosomal Microarray Detection of Constitutional Copy Number Variation Using Saliva DNA
|
Reiner, Jennifer
|
|
2017
|
19 |
3 |
p. 397-403
7 p.
|
artikel
|
| 2 |
Comprehensive Determination of Prostate Tumor ETS Gene Status in Clinical Samples Using the CLIA Decipher Assay
|
Torres, Alba
|
|
2017
|
19 |
3 |
p. 475-484
10 p.
|
artikel
|
| 3 |
Correction
|
|
|
2017
|
19 |
3 |
p. 485-
1 p.
|
artikel
|
| 4 |
Correction
|
|
|
2017
|
19 |
3 |
p. 485-
1 p.
|
artikel
|
| 5 |
Correction
|
|
|
2017
|
19 |
3 |
p. 485-
1 p.
|
artikel
|
| 6 |
Current and Emerging Molecular Tests for Human Papillomavirus–Related Neoplasia in the Genomic Era
|
Leal Jr., Sixto M.
|
|
2017
|
19 |
3 |
p. 366-377
12 p.
|
artikel
|
| 7 |
Detection of Aberrant TERT Promoter Methylation by Combined Bisulfite Restriction Enzyme Analysis for Cancer Diagnosis
|
Lee, Seungjae
|
|
2017
|
19 |
3 |
p. 378-386
9 p.
|
artikel
|
| 8 |
Development and Clinical Utility of a Blood-Based Test Service for the Rapid Identification of Actionable Mutations in Non–Small Cell Lung Carcinoma
|
Mellert, Hestia
|
|
2017
|
19 |
3 |
p. 404-416
13 p.
|
artikel
|
| 9 |
Droplet Digital PCR Is a Reliable Tool for Monitoring Minimal Residual Disease in Acute Promyelocytic Leukemia
|
Brunetti, Claudia
|
|
2017
|
19 |
3 |
p. 437-444
8 p.
|
artikel
|
| 10 |
Editorial Board
|
|
|
2017
|
19 |
3 |
p. A1-A2
nvt p.
|
artikel
|
| 11 |
Guidelines for Validation of Next-Generation Sequencing–Based Oncology Panels
|
Jennings, Lawrence J.
|
|
2017
|
19 |
3 |
p. 341-365
25 p.
|
artikel
|
| 12 |
Haplotype Counting for Sensitive Chimerism Testing
|
Debeljak, Marija
|
|
2017
|
19 |
3 |
p. 427-436
10 p.
|
artikel
|
| 13 |
Identification of NTRK3 Fusions in Childhood Melanocytic Neoplasms
|
Wang, Lu
|
|
2017
|
19 |
3 |
p. 387-396
10 p.
|
artikel
|
| 14 |
Impact of Rapid Molecular Respiratory Virus Testing on Real-Time Decision Making in a Pediatric Emergency Department
|
Rogan, Daniel T.
|
|
2017
|
19 |
3 |
p. 460-467
8 p.
|
artikel
|
| 15 |
Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings
|
Lubin, Ira M.
|
|
2017
|
19 |
3 |
p. 417-426
10 p.
|
artikel
|
| 16 |
Table of Contents
|
|
|
2017
|
19 |
3 |
p. A5-A6
nvt p.
|
artikel
|
| 17 |
Targeted Next-Generation Sequencing of 51 Genes Involved in Primary Electrical Disease
|
Proost, Dorien
|
|
2017
|
19 |
3 |
p. 445-459
15 p.
|
artikel
|
| 18 |
Utilization of Whole-Exome Next-Generation Sequencing Variant Read Frequency for Detection of Lesion-Specific, Somatic Loss of Heterozygosity in a Neurofibromatosis Type 1 Cohort with Tibial Pseudarthrosis
|
Margraf, Rebecca L.
|
|
2017
|
19 |
3 |
p. 468-474
7 p.
|
artikel
|
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