nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A Case of Acute Myeloid Leukemia with Novel Dicentric and Ring of Chromosome 22
|
Cong, Hoang Tran |
|
2016 |
|
5 |
p. 243- 1 p. |
artikel |
2 |
A Case of “Triple-Hit” Lymphoma Diagnosed by Integrated Cytogenetic Approaches: FISH, Karyotyping and Microarray
|
Xu, Dongbin |
|
2016 |
|
5 |
p. 241- 1 p. |
artikel |
3 |
A case with a cytogenetically cryptic variant of the inv(16)(p13q22)/t(16;16)(p13;q22)
|
Van Obbergh, Florence |
|
2014 |
|
5 |
p. 231-232 2 p. |
artikel |
4 |
Acute panmyelosis with myelofibrosis with EVI1 amplification
|
Grygalewicz, Beata |
|
2012 |
|
5 |
p. 255-260 6 p. |
artikel |
5 |
An insertion/deletion polymorphism in the 3′ untranslated region of type I collagen a2 (COL1A2) is associated with susceptibility for hepatocellular carcinoma in a Chinese population
|
Zhu, Zhansheng |
|
2011 |
|
5 |
p. 265-269 5 p. |
artikel |
6 |
An Isogenic Trisomic–Disomic Model System Using Cells from People with Mosaic Down Syndrome Unmasks Trisomy 21 Associated Increases in Age-Related Chromosomal Instability, Senescence Associated Distension of Satellites, and Telomere Shortening
|
Rafferty, Kelly |
|
2016 |
|
5 |
p. 238- 1 p. |
artikel |
7 |
A Novel BCL2 Gene Rearrangement, t(5;18)(q31;q21), in Follicular Lymphoma
|
Kantarci, Sibel |
|
2013 |
|
5 |
p. 212- 1 p. |
artikel |
8 |
A Novel Three-Way Rearrangement Involving ETV6 (12p13) and ABL1 (9q34) in Acute Myeloid Leukemia
|
Siangchin, Ken |
|
2016 |
|
5 |
p. 242- 1 p. |
artikel |
9 |
An Unbalanced Translocation Between Chromosomes 1 and 5 in T-Cell Acute Lymphoblastic Leukemia: A Case Report
|
Cheng, Dongsheng |
|
2016 |
|
5 |
p. 242-243 2 p. |
artikel |
10 |
A Rare Case of Russell-Silver and 1p36 Deletion Syndromes
|
Blackwell, Donna |
|
2016 |
|
5 |
p. 237- 1 p. |
artikel |
11 |
A role for epigenetics in the formation of chromosome translocations in acute leukemia
|
Gill Super, Heidi J. |
|
2015 |
|
5 |
p. 230-236 7 p. |
artikel |
12 |
Assessing Copy Number Variants Involving ACMGG Secondary Finding Genes Identified by Routine Chromosomal SNP Array in a Clinical Pediatric Population
|
Fan, Jinbo |
|
2016 |
|
5 |
p. 230- 1 p. |
artikel |
13 |
Associations of THBS2 and THBS4 polymorphisms to gastric cancer in a Southeast Chinese population
|
Lin, Xiandong |
|
2016 |
|
5 |
p. 215-222 8 p. |
artikel |
14 |
A three-way translocation of MLL, MLLT11, and the novel reciprocal partner gene MYO18A in a child with acute myeloid leukemia
|
Ussowicz, Marek |
|
2012 |
|
5 |
p. 261-265 5 p. |
artikel |
15 |
A Variant of inv(3)(q21q26.2) or t(3;3)(q21;q26.2) (MECOM) Rearrangement in AML
|
Mueller, Rosemary |
|
2016 |
|
5 |
p. 244- 1 p. |
artikel |
16 |
BCR–JAK2 fusion in a myeloproliferative neoplasm with associated eosinophilia
|
He, Rong |
|
2016 |
|
5 |
p. 223-228 6 p. |
artikel |
17 |
Bi-allelic Amplification of ATM Gene in Blastoid Variant of Mantle Cell Lymphoma: A Novel Mechanism of Inactivation Due to Chromothripsis?
|
Mendiola, Christina |
|
2016 |
|
5 |
p. 244- 1 p. |
artikel |
18 |
Case Report of a Complex Supernumerary Chromosome That Represents Constitutional Chromoanagenesis
|
Haddadin, Mary |
|
2016 |
|
5 |
p. 249- 1 p. |
artikel |
19 |
Case Report: Unbalanced Translocation Causing Terminal Deletion of 11q25 to 11qter and Terminal Duplication of 12q24 to 12qter in Addition to 16q24.2 Deletion
|
Abdulwahed, Omaiyah Al |
|
2016 |
|
5 |
p. 248- 1 p. |
artikel |
20 |
Characterization of a Complex Derivative Chromosome 18
|
Penton, Andrea |
|
2016 |
|
5 |
p. 247-248 2 p. |
artikel |
21 |
Characterization of Chromosome Translocation Breakpoints in Leukemia Using Whole Genome Mate-Pair Sequencing
|
Qi, Zhongxia(Joe) |
|
2016 |
|
5 |
p. 236- 1 p. |
artikel |
22 |
Chromosomal Microarray as a First Tier Test Following Diagnostic Prenatal Procedure. The Toronto Mount Sinai Hospital Experience
|
Kolomietz, Elena |
|
2016 |
|
5 |
p. 229-230 2 p. |
artikel |
23 |
Chromosomal translocations involving the IGH@ locus in B-cell precursor acute lymphoblastic leukemia: 29 new cases and a review of the literature
|
Chapiro, Elise |
|
2013 |
|
5 |
p. 162-173 12 p. |
artikel |
24 |
Clinical Impact of Genomic Duplications: A Discussion of Reporting Practices
|
Marcou, Cherisse A. |
|
2016 |
|
5 |
p. 230-231 2 p. |
artikel |
25 |
Clinical Utility of SNP Microarrays in Adult Brain Tumors: Molecular Insight into Tumor Heterogeneity and Progression
|
Znoyko, Iya |
|
2013 |
|
5 |
p. 215- 1 p. |
artikel |
26 |
Clinical Utility of the Detection of Genomic Aberrations in Formalin-Fixed Paraffin-Embedded Myeloid Sarcoma Samples
|
Sukhanova, Madina |
|
2013 |
|
5 |
p. 214-215 2 p. |
artikel |
27 |
Clinical Validation of a Simple FISH Assay That Uses 1 µl of Probe
|
Stanchfield, James |
|
2016 |
|
5 |
p. 249- 1 p. |
artikel |
28 |
CNVs Provide the Clue for a Cryptic t(5;11) in Acute Myeloid Leukemia
|
Chia, Nicole L. |
|
2013 |
|
5 |
p. 211- 1 p. |
artikel |
29 |
Complex Cases: Putting It All Together Using the Tools in Your Toolbox (Microarray, FISH and Chromosome Analysis)
|
Smolarek, Teresa A. |
|
2016 |
|
5 |
p. 230- 1 p. |
artikel |
30 |
Comprehensive BRCA1 and BRCA2 mutational profile in Lithuania
|
Janavičius, Ramūnas |
|
2014 |
|
5 |
p. 195-205 11 p. |
artikel |
31 |
Correlating Copy Number Alterations in Dedifferentiated Liposarcoma With Tumor Behavior and Patient Outcome
|
Liu, Yajuan |
|
2016 |
|
5 |
p. 232- 1 p. |
artikel |
32 |
Correlating Hepatoblastoma Outcome With Karyotype and Microarray Data—A Pilot Study
|
Cooley, Linda |
|
2016 |
|
5 |
p. 242- 1 p. |
artikel |
33 |
Correlation of polypoid colorectal adenocarcinoma with pre-existing adenomatous polyps and KRAS mutation
|
Chen, Hui |
|
2011 |
|
5 |
p. 245-251 7 p. |
artikel |
34 |
Cover 1
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2014 |
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5 |
p. OFC- 1 p. |
artikel |
35 |
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2015 |
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p. OFC- 1 p. |
artikel |
36 |
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2013 |
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p. OFC- 1 p. |
artikel |
37 |
Cover 1
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2012 |
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p. OFC- 1 p. |
artikel |
38 |
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p. OFC- 1 p. |
artikel |
39 |
Cover_spine
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2016 |
|
5 |
p. CO1- 1 p. |
artikel |
40 |
CTLA-4 gene polymorphism at position +49 A>G in exon 1: a risk factor for cervical cancer in Indian women
|
Gokhale, Priyanka |
|
2013 |
|
5 |
p. 154-161 8 p. |
artikel |
41 |
Current state of pediatric sarcoma biology and opportunities for future discovery: A report from the sarcoma translational research workshop
|
Hingorani, Pooja |
|
2016 |
|
5 |
p. 182-194 13 p. |
artikel |
42 |
Cytogenetics of Infant/Congenital Leukemia: Mayo Clinic Experience From 2005–2015
|
Cao, Yang |
|
2016 |
|
5 |
p. 232- 1 p. |
artikel |
43 |
Cytogenetic Studies Supporting the Development of New Immunotherapy for B-cell Acute Lymphoblastic Leukemia
|
Aikawa, Vania |
|
2016 |
|
5 |
p. 233- 1 p. |
artikel |
44 |
Development of a Chromosomal Microarray Test for the Detection of Abnormalities in Formalin-Fixed Paraffin-Embedded Products of Conception Specimens
|
Gliem, Troy J. |
|
2016 |
|
5 |
p. 240-241 2 p. |
artikel |
45 |
Differences in the cytogenetic alteration profiles of diffuse large B-cell lymphoma among Chinese and American patients
|
Chen, Yan |
|
2013 |
|
5 |
p. 183-190 8 p. |
artikel |
46 |
Direct FISH, Cultured Chromosome Analysis, and Direct SNP Microarray Analysis in Identifying Ring Chromosomes on Prenatal Analysis: A Case of 45,X/46,X,r(X)
|
Risheg, Hiba |
|
2016 |
|
5 |
p. 229- 1 p. |
artikel |
47 |
Disturbing the histone code in leukemia: translocations and mutations affecting histone methyl transferases
|
Chopra, Martin |
|
2015 |
|
5 |
p. 192-205 14 p. |
artikel |
48 |
DNA methylation and RNA expression profiles in lung adenocarcinomas of never-smokers
|
Mansfield, Aaron S. |
|
2015 |
|
5 |
p. 253-260 8 p. |
artikel |
49 |
Downregulation of miR-21 increases cisplatin sensitivity of non–small-cell lung cancer
|
Xu, Liyun |
|
2014 |
|
5 |
p. 214-220 7 p. |
artikel |
50 |
Dystrophin and dysferlin double mutant mice: a novel model for rhabdomyosarcoma
|
Hosur, Vishnu |
|
2012 |
|
5 |
p. 232-241 10 p. |
artikel |
51 |
Editorial Board
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2014 |
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5 |
p. IFC- 1 p. |
artikel |
52 |
Editorial Board
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2016 |
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5 |
p. CO2- 1 p. |
artikel |
53 |
Editorial Board
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2015 |
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5 |
p. IFC- 1 p. |
artikel |
54 |
Editorial Board
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2013 |
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5 |
p. IFC- 1 p. |
artikel |
55 |
Editorial Board
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2012 |
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5 |
p. IFC- 1 p. |
artikel |
56 |
Editorial Board
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2011 |
|
5 |
p. IFC- 1 p. |
artikel |
57 |
Epigenetic changes in BRCA1-mutated familial breast cancer
|
Downs, Bradley |
|
2015 |
|
5 |
p. 237-240 4 p. |
artikel |
58 |
Evaluation of a Cystic Placenta: Spectrum of Genomic Changes Including GRB10 Microdeletion
|
Surti, Urvashi |
|
2016 |
|
5 |
p. 231- 1 p. |
artikel |
59 |
Evaluation of the Clinical Utility of Sanger Sequencing Following Next Generation Sequence Analysis
|
Sanmann, Jennifer N. |
|
2016 |
|
5 |
p. 246- 1 p. |
artikel |
60 |
Exon-Targeted Array CGH for Identification of Clinically Relevant Small-Sized, Intragenic CNVs
|
Patel, Ankita |
|
2016 |
|
5 |
p. 239-240 2 p. |
artikel |
61 |
Expression of HOXB genes is significantly different in acute myeloid leukemia with a partial tandem duplication of MLL vs. a MLL translocation: a cross-laboratory study
|
Liu, Hsi-Che |
|
2011 |
|
5 |
p. 252-259 8 p. |
artikel |
62 |
Four Generation Family With a Complex Insertion of 16q in 4p
|
DuPont, Barbara R. |
|
2016 |
|
5 |
p. 236-237 2 p. |
artikel |
63 |
Further evidence for germline BAP1 mutations predisposing to melanoma and malignant mesothelioma
|
Cheung, Mitchell |
|
2013 |
|
5 |
p. 206-210 5 p. |
artikel |
64 |
Gamification of Chromosome Identification: Creation of a Software Tool to Introduce Cytogenetic Analysis
|
Paschal, Cate Randall |
|
2016 |
|
5 |
p. 239- 1 p. |
artikel |
65 |
Genomic imbalances in benign metastasizing leiomyoma: characterization by conventional karyotypic, fluorescence in situ hybridization, and whole genome SNP array analysis
|
Bowen, Joslin M. |
|
2012 |
|
5 |
p. 249-254 6 p. |
artikel |
66 |
Glioblastoma specimens with TP53 mutations do not show EGFRvIII amplification
|
Stoczynska-Fidelus, Ewelina |
|
2011 |
|
5 |
p. 282-283 2 p. |
artikel |
67 |
High frequency of BTG1 deletions in patients with BCR-ABL1–positive acute leukemia
|
Xie, Jundan |
|
2014 |
|
5 |
p. 226-230 5 p. |
artikel |
68 |
High Resolution Genomic Profiling of Metastatic Testicular Teratomas
|
Ouyang, Karen J. |
|
2013 |
|
5 |
p. 213- 1 p. |
artikel |
69 |
High Resolution SNP Microarray Analysis is Useful for Diagnosis and Prognosis of Renal Epithelial Neoplasms
|
Wolff, Daynna J. |
|
2013 |
|
5 |
p. 215- 1 p. |
artikel |
70 |
5-hydroxymethylcytosine in cancer: significance in diagnosis and therapy
|
Vasanthakumar, Aparna |
|
2015 |
|
5 |
p. 167-177 11 p. |
artikel |
71 |
Hypermethylation of the CpG dinucleotide in epidermal growth factor receptor codon 790: implications for a mutational hotspot leading to the T790M mutation in non–small-cell lung cancer
|
Fujii, Akiko |
|
2015 |
|
5 |
p. 271-278 8 p. |
artikel |
72 |
Identification of genetic susceptibility to childhood cancer through analysis of genes in parallel
|
|
|
2011 |
|
5 |
p. 284- 1 p. |
artikel |
73 |
Identification of the prevalent BRCA1 and BRCA2 mutations in the female population of Puerto Rico
|
Dutil, Julie |
|
2012 |
|
5 |
p. 242-248 7 p. |
artikel |
74 |
Incidental Findings Found in Whole Genome SNP Microarray Analysis in Both Prenatal and Oncology Studies
|
Schwartz, Stuart |
|
2016 |
|
5 |
p. 233-234 2 p. |
artikel |
75 |
Increased copy number of the DLX4 homeobox gene in breast axillary lymph node metastasis
|
Torresan, Clarissa |
|
2014 |
|
5 |
p. 177-187 11 p. |
artikel |
76 |
Increased sperm aneuploidy in two male carriers of germline TP53 mutations
|
Paulasova, Petra |
|
2011 |
|
5 |
p. 278-281 4 p. |
artikel |
77 |
Inheritance and Phase Determination in a Patient With Early Onset Parkinson Disease and Two PARK2 Deletions
|
Williams, Eli S. |
|
2016 |
|
5 |
p. 240- 1 p. |
artikel |
78 |
Inhibition of the mevalonate pathway affects epigenetic regulation in cancer cells
|
Karlic, Heidrun |
|
2015 |
|
5 |
p. 241-252 12 p. |
artikel |
79 |
Integrated high-resolution array CGH and SKY analysis of homozygous deletions and other genomic alterations present in malignant mesothelioma cell lines
|
Klorin, Geula |
|
2013 |
|
5 |
p. 191-205 15 p. |
artikel |
80 |
Integrative analysis of copy number alteration and gene expression profiling in ovarian clear cell adenocarcinoma
|
Sung, Chang Ohk |
|
2013 |
|
5 |
p. 145-153 9 p. |
artikel |
81 |
Interpreting Complex SNP-Array Results in Tumors: Clues Invoking Classical Cytogenetic Mechanisms
|
Rowsey, Ross A. |
|
2016 |
|
5 |
p. 234- 1 p. |
artikel |
82 |
Introduction to progress and promise of epigenetics for diagnosis and therapy in cancer
|
Zeleznik-Le, Nancy J. |
|
2015 |
|
5 |
p. 165-166 2 p. |
artikel |
83 |
Is Intrachromosomal Amplification of Chromosome 21 (iAMP21) Always Intrachromosomal?
|
Tsuchiya, Karen |
|
2016 |
|
5 |
p. 231-232 2 p. |
artikel |
84 |
Isolated Sex Chromosome Loss after Allogeneic Stem Cell Transplant in Patients With Hematological Malignancies
|
Tang, Zhenya |
|
2016 |
|
5 |
p. 241- 1 p. |
artikel |
85 |
It's Not You, It's Me: Somatic and Germline Mutations Detected Through Routine Clinical Testing
|
Morrissette, Jennifer |
|
2016 |
|
5 |
p. 234-235 2 p. |
artikel |
86 |
Jumping-like translocation—a rare chromosomal rearrangement in a patient with Burkitt lymphoma/leukemia
|
Sarova, Iveta |
|
2014 |
|
5 |
p. 221-225 5 p. |
artikel |
87 |
Massive Parallel Sequencing of Leukemia Samples Using a Custom Designed Cancer Gene Mutation Panel
|
Chang, Fengqi |
|
2013 |
|
5 |
p. 211- 1 p. |
artikel |
88 |
Microarray Analysis of Formalin-Fixed Paraffin-Embedded (FFPET) and Frozen (FZT) Uveal Melanoma Detects Clinically Relevant Abnormalities, Including Chromosome 3 Loss of Heterozygosity
|
Schultz, Roger A. |
|
2013 |
|
5 |
p. 214- 1 p. |
artikel |
89 |
Microarray and Next Generation Sequencing: Complementary Technologies for Diagnosing Autosomal Recessive Disorders
|
Chaubey, Alka |
|
2016 |
|
5 |
p. 239- 1 p. |
artikel |
90 |
Microarray Studies in Pediatric T-Cell Acute Lymphoblastic Leukemia/Lymphoma: A Report of Four Cases
|
Sanmann, Jennifer N. |
|
2013 |
|
5 |
p. 213- 1 p. |
artikel |
91 |
Microdeletion of ZBTB20 Results in a Phenotype Overlapping With That of the Microdeletion 3q13.31 Syndrome
|
Mulatinho, Milene |
|
2016 |
|
5 |
p. 244-245 2 p. |
artikel |
92 |
MicroRNA profiling with correlation to gene expression revealed the oncogenic miR-17-92 cluster to be up-regulated in osteosarcoma
|
Baumhoer, Daniel |
|
2012 |
|
5 |
p. 212-219 8 p. |
artikel |
93 |
Molecular characterization of a t(2;7) translocation linking CDK6 to the IGK locus in CD5− monoclonal B-cell lymphocytosis
|
Parker, Edward |
|
2011 |
|
5 |
p. 260-264 5 p. |
artikel |
94 |
Molecular Inversion Probes for Detection of Copy Number Alterations and Loss of Heterozygosity in Renal Cell Carcinoma
|
Jobanputra, Vaidehi |
|
2013 |
|
5 |
p. 212- 1 p. |
artikel |
95 |
Molecular pathology and its diagnostic use in bone tumors
|
Szuhai, Karoly |
|
2012 |
|
5 |
p. 193-204 12 p. |
artikel |
96 |
Multiple CDK/CYCLIND genes are amplified in medulloblastoma and supratentorial primitive neuroectodermal brain tumor
|
Li, Meihua |
|
2012 |
|
5 |
p. 220-231 12 p. |
artikel |
97 |
Mutation analysis of the PALB2 gene in unselected pancreatic cancer patients in the Czech Republic
|
Borecka, M. |
|
2016 |
|
5 |
p. 199-204 6 p. |
artikel |
98 |
Mutation Profiling of Clinical Tumor Samples Using Next Generation Sequencing
|
Liu, Liu |
|
2013 |
|
5 |
p. 213- 1 p. |
artikel |
99 |
MYC Gene Rearrangement in Plasma Cell Neoplasms
|
Biggerstaff, Julie Sanford |
|
2016 |
|
5 |
p. 235-236 2 p. |
artikel |
100 |
New Genetic Alterations in Pediatric Acute Lymphoblastic Leukemia Uncovered by Chromosomal Microarray Analysis
|
Gaskin, Shannon |
|
2016 |
|
5 |
p. 234- 1 p. |
artikel |
101 |
Next Generation Cytogenetics: Genome-wide Mate Pair Sequencing for Detection of Structural Rearrangements and Copy Number Variation
|
Aypar, Umut |
|
2016 |
|
5 |
p. 234- 1 p. |
artikel |
102 |
Next Generation Interphase Chromosome Profiling (NextGen ICP): Proof-of-Concept of Novel Technology
|
Babu, Ramesh |
|
2016 |
|
5 |
p. 247- 1 p. |
artikel |
103 |
Non-Invasive Prenatal Screening of Over 200,000 Tests Performed at Natera
|
Zneimer, Susan |
|
2016 |
|
5 |
p. 238- 1 p. |
artikel |
104 |
Novel Cytogenetic Findings in a Case of Mixed Phenotype Acute Leukemia With a Complex Karyotype
|
Shabsovich, David |
|
2016 |
|
5 |
p. 242- 1 p. |
artikel |
105 |
Optimizing Array Design and Content for the Modern Cytogenetic Research Lab
|
Chin, Ephrem |
|
2016 |
|
5 |
p. 246- 1 p. |
artikel |
106 |
Over-expression of prolyl hydroxylase-1 blocks NF-κB-mediated cyclin D1 expression and proliferation in lung carcinoma cells
|
Xie, Xiao |
|
2014 |
|
5 |
p. 188-194 7 p. |
artikel |
107 |
Pediatric leukemia predisposition syndromes: clues to understanding leukemogenesis
|
Seif, Alix E. |
|
2011 |
|
5 |
p. 227-244 18 p. |
artikel |
108 |
Performance of the Genomic DNA Assay for the Agilent 4200 TapeStation System
|
Nitsche, Rainer |
|
2016 |
|
5 |
p. 249- 1 p. |
artikel |
109 |
Poly (AT) polymorphism in the XPC gene and smoking enhance the risk of prostate cancer in a low-risk Chinese population
|
Liu, Yang |
|
2012 |
|
5 |
p. 205-211 7 p. |
artikel |
110 |
Precision Medicine for Autism and Related Developmental Brain Disorders
|
Ledbetter, David |
|
2016 |
|
5 |
p. 239- 1 p. |
artikel |
111 |
Predictive chromosomal clusters of synchronous and metachronous brain metastases in clear cell renal cell carcinoma
|
Gutenberg, Angelika |
|
2014 |
|
5 |
p. 206-213 8 p. |
artikel |
112 |
Prenatal SNP Microarray Analysis and Parental Follow-up of 16q24.1 Deletions That Include the FOXF1 Gene
|
Schleede, Justin |
|
2016 |
|
5 |
p. 248- 1 p. |
artikel |
113 |
Pre-Phase Chemotherapy for Acute Lymphoblastic Leukemia: A Cautionary Tale
|
Arreola, Alexandra |
|
2016 |
|
5 |
p. 241- 1 p. |
artikel |
114 |
Promoter hypermethylation of membrane type 3 matrix metalloproteinase is associated with cell migration in colorectal adenocarcinoma
|
Moon, Ji Wook |
|
2015 |
|
5 |
p. 261-270 10 p. |
artikel |
115 |
Publisher's note
|
Ruimy, Anne |
|
2016 |
|
5 |
p. 179-181 3 p. |
artikel |
116 |
Rare Focal Deletions Involving SNRPN and UBE3A Genes
|
Meck, Jeanne |
|
2016 |
|
5 |
p. 238- 1 p. |
artikel |
117 |
Re-Examination of Danish Carriers of Balanced Chromosomal Inversions
|
Rasmussen, Malene B. |
|
2016 |
|
5 |
p. 231- 1 p. |
artikel |
118 |
Regulatory Mutations of FOXG1 in the Context of Topological Domains
|
Mehrjouy, Mana M. |
|
2016 |
|
5 |
p. 245- 1 p. |
artikel |
119 |
SH2B3 Aberrations Enriched in iAMP21 B Lymphoblastic Leukemia Cohort
|
Baughn, Linda |
|
2016 |
|
5 |
p. 236- 1 p. |
artikel |
120 |
SOSTDC1 down-regulation of expression involves CpG methylation and is a potential prognostic marker in gastric cancer
|
Gopal, Gopisetty |
|
2013 |
|
5 |
p. 174-182 9 p. |
artikel |
121 |
Table of Contents
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|
2014 |
|
5 |
p. A1- 1 p. |
artikel |
122 |
Table of Contents
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2016 |
|
5 |
p. A1- 1 p. |
artikel |
123 |
Table of Contents
|
|
|
2015 |
|
5 |
p. A1- 1 p. |
artikel |
124 |
Table of Contents
|
|
|
2012 |
|
5 |
p. A1- 1 p. |
artikel |
125 |
Table of Contents
|
|
|
2013 |
|
5 |
p. A1- 1 p. |
artikel |
126 |
Table of Contents
|
|
|
2011 |
|
5 |
p. A1-A2 nvt p. |
artikel |
127 |
The ABL and JAK Tyrosine Kinase Pathways May be Co-Activated in a Subset of BCR/ABL1 Positive Acute Lymphoid Leukemia
|
Aviv, Hana |
|
2016 |
|
5 |
p. 235- 1 p. |
artikel |
128 |
The cancer COMPASS: navigating the functions of MLL complexes in cancer
|
Ford, David J. |
|
2015 |
|
5 |
p. 178-191 14 p. |
artikel |
129 |
The Clinical Spectrum Associated With Xq25q26 Duplications: A Report of Two Novel Duplications and Review of the Literature
|
Herriges, John |
|
2016 |
|
5 |
p. 246-247 2 p. |
artikel |
130 |
The Effective Use of the Cancer Genome Atlas (TCGA) Data by the Cancer Cytogenetic Community
|
Shams, Soheil |
|
2013 |
|
5 |
p. 214- 1 p. |
artikel |
131 |
The effect of TP53 codon 72 and RNASEL codon 462 polymorphisms on the development of cervical cancer in Argentine women
|
Barbisan, Gisela |
|
2011 |
|
5 |
p. 270-277 8 p. |
artikel |
132 |
The pathological role and prognostic impact of miR-181 in acute myeloid leukemia
|
Weng, Hengyou |
|
2015 |
|
5 |
p. 225-229 5 p. |
artikel |
133 |
The potential utility of re-mining results of somatic mutation testing: KRAS status in lung adenocarcinoma
|
Biernacka, Anna |
|
2016 |
|
5 |
p. 195-198 4 p. |
artikel |
134 |
The prognostic significance of an inv(3)(q21q26.2) in addition to a t(9;22)(q34;q11.2) in patients treated with tyrosine kinase inhibitors
|
Theil, Karl S. |
|
2014 |
|
5 |
p. 171-176 6 p. |
artikel |
135 |
The role of the histone demethylase KDM4A in cancer
|
Guerra-Calderas, Lissania |
|
2015 |
|
5 |
p. 215-224 10 p. |
artikel |
136 |
The roles of chromatin-remodelers and epigenetic modifiers in kidney cancer
|
Liao, Lili |
|
2015 |
|
5 |
p. 206-214 9 p. |
artikel |
137 |
The t(12;21) Translocation in the Context of a Complex Karyotype in Pediatric B-ALL
|
Buchanan, Justin |
|
2016 |
|
5 |
p. 243-244 2 p. |
artikel |
138 |
The Use of Next Generation Sequencing in the Evaluation of Myeloid Neoplasms: A Comparison with Cytogenetics
|
Williams, Eli S. |
|
2016 |
|
5 |
p. 232-233 2 p. |
artikel |
139 |
Title—TBD
|
Pinkel, Daniel |
|
2016 |
|
5 |
p. 235- 1 p. |
artikel |
140 |
Triploidy in a Live-Born Female With Normal Non-Invasive Prenatal Testing Results
|
Wheeler, Ferrin C. |
|
2016 |
|
5 |
p. 245-246 2 p. |
artikel |
141 |
Trisomy 12 and Triploidy in an Infant: An Unusual Case of Diploid/Triploid Mixoploidy
|
Matyakhina, Ludmila |
|
2016 |
|
5 |
p. 248-249 2 p. |
artikel |
142 |
Trisomy 12 Mosaicism Detected by Genomic Microarray in a Newborn Child
|
Hong, Bo |
|
2016 |
|
5 |
p. 247- 1 p. |
artikel |
143 |
Two new Translocations Involving RUNX1
|
Bruyere, Helene |
|
2016 |
|
5 |
p. 243- 1 p. |
artikel |
144 |
Unexpected Chromosomal Abnormalities Identified by CMA Confirmation Studies
|
Cheung, Sau W. |
|
2016 |
|
5 |
p. 239- 1 p. |
artikel |
145 |
Unique Challenges and Discoveries From Chromosome Genomic Array Testing (CGAT) in the Setting of Hematopoietic Cell Transplantation
|
Fang, Min |
|
2013 |
|
5 |
p. 212- 1 p. |
artikel |
146 |
WEE1 is a validated target of the microRNA miR-17-92 cluster in leukemia
|
Brockway, Sonia |
|
2015 |
|
5 |
p. 279-287 9 p. |
artikel |
147 |
What Elephants Can Teach Us About Preventing Cancer in Humans
|
Schiffman, Joshua D. |
|
2016 |
|
5 |
p. 236- 1 p. |
artikel |
148 |
Whole-arm translocation of der(5;17)(p10;q10) with concurrent TP53 mutations in acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS): A unique molecular-cytogenetic subgroup
|
Hong, Ming |
|
2016 |
|
5 |
p. 205-214 10 p. |
artikel |
149 |
Why Chromosomes Are Relevant
|
Cherry, Athena M. |
|
2016 |
|
5 |
p. 237- 1 p. |
artikel |