| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acquisition of a t(11;14)(q13;q32) in clonal evolution in a follicular lymphoma with a t(14;18)(q32;q21) and t(3;22)(q27;q11.2)
|
Koduru, Prasad R.
|
|
2015
|
208 |
6 |
p. 303-309
7 p.
|
artikel
|
| 2 |
Amplified Allelic Imbalance – A Genetic Signature of Malignant Peripheral Nerve Sheath Tumors (MPNST)
|
Znoyko, Iya Y.
|
|
2015
|
208 |
6 |
p. 358-
1 p.
|
artikel
|
| 3 |
Analytical Validation of Chromosomal Microarray Analysis with Solid Tumor FFPE Specimens
|
Lefferts, Joel A.
|
|
2015
|
208 |
6 |
p. 360-361
2 p.
|
artikel
|
| 4 |
A Novel Mutation in Calreticulin (CALR) was Identified in a Patient of African American Origin with Thrombocytosis
|
Dash, D.P.
|
|
2015
|
208 |
6 |
p. 363-
1 p.
|
artikel
|
| 5 |
ARID1A and TERT promoter mutations in dedifferentiated meningioma
|
Abedalthagafi, Malak S.
|
|
2015
|
208 |
6 |
p. 345-350
6 p.
|
artikel
|
| 6 |
Array CGH and Conventional Karyotyping: The Description of Two Selected Cases
|
Barbato, Ingrid T.
|
|
2015
|
208 |
6 |
p. 362-363
2 p.
|
artikel
|
| 7 |
Bilateral Radial Ray Defects: An Atypical Presentation of 16p11.2 Microdeletion Syndrome
|
Vallee, Stephanie E.
|
|
2015
|
208 |
6 |
p. 365-
1 p.
|
artikel
|
| 8 |
BRAF V600E mutations: a series of case reports in patients with non–small cell lung cancer
|
Goldman, Jamie M.
|
|
2015
|
208 |
6 |
p. 351-354
4 p.
|
artikel
|
| 9 |
Clinical Validation and Implementation of a Targeted Sequencing Panel for Predisposition to Inherited Cancer
|
Turner, Scott A.
|
|
2015
|
208 |
6 |
p. 362-
1 p.
|
artikel
|
| 10 |
Clinico- and Pathogenomic Analyses of a Single Institution Diffuse Large B-Cell Lymphoma Cohort
|
Guttapalli, Asha
|
|
2015
|
208 |
6 |
p. 357-358
2 p.
|
artikel
|
| 11 |
Complex Syndactyly and Atypical Ectrodactyly in a Child with a Mosaic Karyotype Involving Trisomy 21 and Partial Duplication of Chromosome 21
|
Enchautegui-Colon, Yazmin
|
|
2015
|
208 |
6 |
p. 364-
1 p.
|
artikel
|
| 12 |
Comprehensive evaluation of the effectiveness of gene expression signatures to predict complete response to neoadjuvant chemoradiotherapy and guide surgical intervention in rectal cancer
|
Lopes-Ramos, Camila
|
|
2015
|
208 |
6 |
p. 319-326
8 p.
|
artikel
|
| 13 |
Congenital Heart Defects in Neonates: Determining the Incidence of Genetic Testing and Follow-up Consultation at UCLA
|
Kantarci, Sibel
|
|
2015
|
208 |
6 |
p. 359-
1 p.
|
artikel
|
| 14 |
Cover 1
|
|
|
2015
|
208 |
6 |
p. OFC-
1 p.
|
artikel
|
| 15 |
Editorial Board
|
|
|
2015
|
208 |
6 |
p. A1-
1 p.
|
artikel
|
| 16 |
Evaluation of SNP Genomic Microarray Analysis as an Alternative to FISH Analysis of Pediatric Solid Tumors
|
Arnoldo, Anthony
|
|
2015
|
208 |
6 |
p. 361-362
2 p.
|
artikel
|
| 17 |
Genomic profile of a Li-Fraumeni-like syndrome patient with a 45,X/46,XX karyotype, presenting neither mutations in TP53 nor clinical stigmata of Turner syndrome
|
Basso, Tatiane R.
|
|
2015
|
208 |
6 |
p. 341-344
4 p.
|
artikel
|
| 18 |
Implementation and Routine Clinical Use of the TruSight Myeloid Sequencing Panel in Patients with Myeloid Malignancies
|
Peterson, Jason D.
|
|
2015
|
208 |
6 |
p. 361-
1 p.
|
artikel
|
| 19 |
Increased LOH Resolution Achieved with the Addition of Comprehensive and Updated SNP Content on Agilent’s CGH +SNP Cancer and Postnatal Array Platform
|
Dutta, Anindita
|
|
2015
|
208 |
6 |
p. 364-
1 p.
|
artikel
|
| 20 |
International Breakpoint Mapping Consortium (IBMC). Systematic Mapping of Chromosomal Breakpoints in the Context of Phenotypes and Nuclear Genome Organization
|
Tommerup, Niels
|
|
2015
|
208 |
6 |
p. 359-360
2 p.
|
artikel
|
| 21 |
Large Cryptic Derivative Chromosome 8 Detected by SNP Chromosomal Microarray
|
Jacques, Heather
|
|
2015
|
208 |
6 |
p. 365-
1 p.
|
artikel
|
| 22 |
Microdissecting the role of microRNAs in the pathogenesis of prostate cancer
|
Ayub, Shiekh Gazalla
|
|
2015
|
208 |
6 |
p. 289-302
14 p.
|
artikel
|
| 23 |
Petabyte-Scale Cancer Genomics in the Cloud
|
Davis-Dusenbery, Brandi N.
|
|
2015
|
208 |
6 |
p. 360-
1 p.
|
artikel
|
| 24 |
Postnatal Chromosomal Microarray Reveals a False Positive Trisomy 21 NIPS Result
|
Cao, Yang
|
|
2015
|
208 |
6 |
p. 357-
1 p.
|
artikel
|
| 25 |
Rare Double-Hit with Two Translocations Involving IgH Both with BCL2 and BCL3 in a Monoclonal B-Cell Leukemia
|
Alpatov, Roman
|
|
2015
|
208 |
6 |
p. 362-
1 p.
|
artikel
|
| 26 |
Retrospective evaluation of the clinical and laboratory data from 300 patients of various hematological malignancies with chromosome 3 abnormalities
|
Liu, Dandan
|
|
2015
|
208 |
6 |
p. 333-340
8 p.
|
artikel
|
| 27 |
Single nucleotide polymorphisms of the NF-κB and STAT3 signaling pathway genes predict lung cancer prognosis in a Chinese Han population
|
He, Fei
|
|
2015
|
208 |
6 |
p. 310-318
9 p.
|
artikel
|
| 28 |
Streamlining NGS Workflows Using Cancer Samples by the Application of Tthe DNA Integrity Number (DIN) from the Genomic DNA Screentape Assay
|
Borg, Solange
|
|
2015
|
208 |
6 |
p. 365-
1 p.
|
artikel
|
| 29 |
Table of Contents
|
|
|
2015
|
208 |
6 |
p. A2-A3
nvt p.
|
artikel
|
| 30 |
Terminal Gain of 12p13.33 and Terminal Loss of 9p24.3, Detected in a Child with Developmental Delay and Growth Issues and Due to a Maternal Unbalanced Rearrangement Between 12p and 9p
|
Haag, Mary M.
|
|
2015
|
208 |
6 |
p. 364-
1 p.
|
artikel
|
| 31 |
The lack of E318K MITF germline mutation in Latvian melanoma patients
|
Ozola, Aija
|
|
2015
|
208 |
6 |
p. 355-356
2 p.
|
artikel
|
| 32 |
The Smallest Reported Distal 11q25 Deletion in Jacobsen Syndrome (JBS): Two Patients with Variable Phenotype
|
Zhang, Lei
|
|
2015
|
208 |
6 |
p. 360-
1 p.
|
artikel
|
| 33 |
Transcriptome Analysis (Rnaseq) Detects Gene Fusions and Point Mutations Associated with Ph-Like Acute Lymphoblastic Leukemia
|
Yap, Kai Lee
|
|
2015
|
208 |
6 |
p. 358-
1 p.
|
artikel
|
| 34 |
Unusual ROS1 Translocation Pattern in a 61 Year-old Woman with Metastatic Adenocarcinoma of Lung
|
Chen, Hui
|
|
2015
|
208 |
6 |
p. 363-
1 p.
|
artikel
|
| 35 |
Validation of a Modified OncoScan Protocol for Use in a Clinical Laboratory
|
Paxton, Christian N.
|
|
2015
|
208 |
6 |
p. 361-
1 p.
|
artikel
|
| 36 |
WHIM Syndrome Cured by Chromothripsis
|
Bryke, Christine R.
|
|
2015
|
208 |
6 |
p. 358-359
2 p.
|
artikel
|
| 37 |
Whole exome sequencing in a case of sporadic multiple meningioma reveals shared NF2, FAM109B, and TPRXL mutations, together with unique SMARCB1 alterations in a subset of tumor nodules
|
Torres-Martín, Miguel
|
|
2015
|
208 |
6 |
p. 327-332
6 p.
|
artikel
|
| 38 |
Y Chromosome Microdeletion Detection by Cytoscan HD Microarray Platform
|
Sederberg, Maria C.
|
|
2015
|
208 |
6 |
p. 359-
1 p.
|
artikel
|
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