| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Accurate Sample Assignment in a Multiplexed, Ultrasensitive, High-Throughput Sequencing Assay for Minimal Residual Disease
|
Bartram, Jack
|
|
2016
|
18 |
4 |
p. 494-506
13 p.
|
artikel
|
| 2 |
A Rapid and Sensitive Next-Generation Sequencing Method to Detect RB1 Mutations Improves Care for Retinoblastoma Patients and Their Families
|
Li, Wenhui L.
|
|
2016
|
18 |
4 |
p. 480-493
14 p.
|
artikel
|
| 3 |
Comparative Evaluation of Four Real-Time PCR Methods for the Quantitative Detection of Epstein-Barr Virus from Whole Blood Specimens
|
Buelow, Daelynn
|
|
2016
|
18 |
4 |
p. 527-534
8 p.
|
artikel
|
| 4 |
Detection of Colorectal Cancer Using a Simplified SEPT9 Gene Methylation Assay Is a Reliable Method for Opportunistic Screening
|
Wu, Dong
|
|
2016
|
18 |
4 |
p. 535-545
11 p.
|
artikel
|
| 5 |
Detection of Germline Mutation in Hereditary Breast and/or Ovarian Cancers by Next-Generation Sequencing on a Four-Gene Panel
|
Kwong, Ava
|
|
2016
|
18 |
4 |
p. 580-594
15 p.
|
artikel
|
| 6 |
Development and Validation of a Mass Spectrometry–Based Assay for the Molecular Diagnosis of Mucin-1 Kidney Disease
|
Blumenstiel, Brendan
|
|
2016
|
18 |
4 |
p. 566-571
6 p.
|
artikel
|
| 7 |
Driver Gene Mutations in Stools of Colorectal Carcinoma Patients Detected by Targeted Next-Generation Sequencing
|
Armengol, Gemma
|
|
2016
|
18 |
4 |
p. 471-479
9 p.
|
artikel
|
| 8 |
Editorial Board
|
|
|
2016
|
18 |
4 |
p. A1-A2
nvt p.
|
artikel
|
| 9 |
Genome-Wide Single-Nucleotide Polymorphism Array Analysis Improves Prognostication of Acute Lymphoblastic Leukemia/Lymphoma
|
Wang, Yunhong
|
|
2016
|
18 |
4 |
p. 595-603
9 p.
|
artikel
|
| 10 |
Hybridization-Induced Aggregation Technology for Practical Clinical Testing
|
Sloane, Hillary S.
|
|
2016
|
18 |
4 |
p. 546-553
8 p.
|
artikel
|
| 11 |
Molecular Cytogenetic Analysis of JAZF1, PHF1, and YWHAE in Endometrial Stromal Tumors
|
Hodge, Jennelle C.
|
|
2016
|
18 |
4 |
p. 516-526
11 p.
|
artikel
|
| 12 |
Multi-Institutional FASTQ File Exchange as a Means of Proficiency Testing for Next-Generation Sequencing Bioinformatics and Variant Interpretation
|
Davies, Kurtis D.
|
|
2016
|
18 |
4 |
p. 572-579
8 p.
|
artikel
|
| 13 |
Next-Generation Proficiency Testing
|
Segal, Jeremy P.
|
|
2016
|
18 |
4 |
p. 469-470
2 p.
|
artikel
|
| 14 |
Table of Contents
|
|
|
2016
|
18 |
4 |
p. A5-
1 p.
|
artikel
|
| 15 |
The Impact on Genetic Testing of Mutational Patterns of CFTR Gene in Different Clinical Macrocategories of Cystic Fibrosis
|
Lucarelli, Marco
|
|
2016
|
18 |
4 |
p. 554-565
12 p.
|
artikel
|
| 16 |
Validation and Implementation of a Custom Next-Generation Sequencing Clinical Assay for Hematologic Malignancies
|
Kluk, Michael J.
|
|
2016
|
18 |
4 |
p. 507-515
9 p.
|
artikel
|
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