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                             43 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A case of acute myeloid leukemia initially treated as chronic lymphocytic leukemia: what do we know about t(4;12)(q12;p13)? Al-Kali, Aref
2010
203 2 p. 348-351
4 p.
artikel
2 Acute myeloid leukemia associated with t(1;3)(p36;q21) and extreme thrombocytosis: a clinical study with literature review Lim, Gayoung
2010
203 2 p. 187-192
6 p.
artikel
3 A novel t(10;12)(q21;p13) involving ETV6 in a patient with acute myeloid leukemia Sowa, Anna S.
2010
203 2 p. 352-354
3 p.
artikel
4 A pericentric inv(9)(p22q34) of the der(9)t(9;22)(q34;q11.2) is a recurrent secondary anomaly in Ph-positive leukemia Pan, Jinlan
2010
203 2 p. 333-340
8 p.
artikel
5 B lymphoblastic leukemia with ETV6 amplification Chae, Hyojin
2010
203 2 p. 284-287
4 p.
artikel
6 Chromosomal alterations in Malaysian patients with nasopharyngeal carcinoma analyzed by comparative genomic hybridization Natasya Naili, M.N.
2010
203 2 p. 309-312
4 p.
artikel
7 Chromosomal imbalances in urinary bladder paraganglioma Schaefer, Inga-Marie
2010
203 2 p. 341-344
4 p.
artikel
8 Clonal heterogeneity and chromosomal instability at disease presentation in high hyperdiploid acute lymphoblastic leukemia Talamo, Anna
2010
203 2 p. 209-214
6 p.
artikel
9 Correlation between clinical characteristics, survival and genetic alterations in patients with hepatocellular carcinoma from Saudi Arabia Al-Qahtani, Ahmed
2010
203 2 p. 269-277
9 p.
artikel
10 Correlation of cytomorphology, immunophenotyping, and interphase fluorescence in situ hybridization in 381 patients with monoclonal gammopathy of undetermined significance and 301 patients with plasma cell myeloma Bacher, Ulrike
2010
203 2 p. 169-175
7 p.
artikel
11 Cytogenetic features of 5q deletion and 5q− syndrome in myelodysplastic syndrome in Korea; marker chromosomes proved to be chromosome 5 with interstitial deletion by fluorescence in situ hybridization Lee, Hye Ryun
2010
203 2 p. 193-202
10 p.
artikel
12 Cytogenetics and genetics of human cancer: methods and accomplishments Sandberg, Avery A.
2010
203 2 p. 102-126
25 p.
artikel
13 Editorial Board 2010
203 2 p. IFC-
1 p.
artikel
14 Editorial Communication Sandberg, Avery A.
2010
203 2 p. 101-
1 p.
artikel
15 EGFR expression and gene copy number in triple-negative breast carcinoma Gumuskaya, Berrak
2010
203 2 p. 222-229
8 p.
artikel
16 Evaluation of upper urinary tract tumors by FISH in Chinese patients Shan, Zhengfei
2010
203 2 p. 238-246
9 p.
artikel
17 Examination of copy number variations of CHST9 in multiple types of hematologic malignancies Zhao, Xiaosu
2010
203 2 p. 176-179
4 p.
artikel
18 FISH-negative cryptic PML–RARA rearrangement detected by long-distance polymerase chain reaction and sequencing analyses: a case study and review of the literature Kim, Min Jin
2010
203 2 p. 278-283
6 p.
artikel
19 FLT3-internal tandem duplication in a pediatric patient with t(8;21) acute myeloid leukemia Kawamura, Machiko
2010
203 2 p. 292-296
5 p.
artikel
20 Gene dosage effects in chronic lymphocytic leukemia Sellmann, Ludger
2010
203 2 p. 149-160
12 p.
artikel
21 Germline mutations of BRCA1 and BRCA2 genes in Turkish breast, ovarian, and prostate cancer patients Manguoğlu, Esra
2010
203 2 p. 230-237
8 p.
artikel
22 GSTT1 copy number gain is a poor predictive marker for escalated-dose imatinib treatment in chronic myeloid leukemia: genetic predictive marker found using array comparative genomic hybridization Koh, Youngil
2010
203 2 p. 215-221
7 p.
artikel
23 Human fetal/tumor metakaryotic stem cells: pangenomic homologous pairing and telomeric end-joining of chromatids Gruhl, Amanda N.
2010
203 2 p. 203-208
6 p.
artikel
24 Letter to the Editor regarding the article “Chromosome abnormalities additional to the Philadelphia chromosome at the diagnosis of chronic myelogenous leukemia: pathogenic and prognostic implications” Najfeld, Vesna
2010
203 2 p. 355-356
2 p.
artikel
25 MicroRNA in chronic lymphocytic leukemia: transitioning from laboratory-based investigation to clinical application Nana-Sinkam, S. Patrick
2010
203 2 p. 127-133
7 p.
artikel
26 Myelodysplastic syndrome with isochromosome 5p and trisomy 8 after treatment of a multiple myeloma Jimenez-Sousa, Maria Angeles
2010
203 2 p. 345-347
3 p.
artikel
27 Numerical chromosomal changes and risk of development of myelodysplastic syndrome–acute myeloid leukemia in patients with Fanconi anemia Mehta, Parinda A.
2010
203 2 p. 180-186
7 p.
artikel
28 6p21 rearrangements in uterine leiomyomas targeting HMGA1 Nezhad, Maliheh Hashemi
2010
203 2 p. 247-252
6 p.
artikel
29 Progressive but previously untreated CLL patients with greater array CGH complexity exhibit a less durable response to chemoimmunotherapy Kay, Neil E.
2010
203 2 p. 161-168
8 p.
artikel
30 Response to the letter by Najfeld regarding the article “Chromosome abnormalities additional to the Philadelphia chromosome at the diagnosis of chronic myelogenous leukemia: pathogenetic and prognostic implications” Zaccaria, Alfonso
2010
203 2 p. 357-
1 p.
artikel
31 Response to Zaccaria regarding the article “Chromosome abnormalities additional to the Philadelphia chromosome at the diagnosis of chronic myelogenous leukemia: pathogenetic and prognostic implications” Najfeld, Vesna
2010
203 2 p. 358-
1 p.
artikel
32 Role of TP53 Arg72Pro polymorphism in urinary bladder cancer predisposition and predictive impact of proline related genotype in advanced tumors in an ethnic Kashmiri population Pandith, Arshad A.
2010
203 2 p. 263-268
6 p.
artikel
33 Screening for common copy-number variants in cancer genes Tyson, Jess
2010
203 2 p. 316-323
8 p.
artikel
34 Screening for DNA copy number aberrations in mucinous adenocarcinoma arising from the minor salivary gland: two case reports Uchida, Kenichiro
2010
203 2 p. 324-327
4 p.
artikel
35 Standardization of fluorescence in situ hybridization studies on chronic lymphocytic leukemia (CLL) blood and marrow cells by the CLL Research Consortium Smoley, Stephanie A.
2010
203 2 p. 141-148
8 p.
artikel
36 Stimulation of chronic lymphocytic leukemia cells with CpG oligodeoxynucleotide gives consistent karyotypic results among laboratories: a CLL Research Consortium (CRC) Study Heerema, Nyla A.
2010
203 2 p. 134-140
7 p.
artikel
37 Table of Contents 2010
203 2 p. A1-A4
nvt p.
artikel
38 Therapy-related acute myeloid leukemia with t(2;11)(q37;q23) after treatment for osteosarcoma Bielorai, Bella
2010
203 2 p. 288-291
4 p.
artikel
39 The t(6;9)(p22;q34) in myeloid neoplasms: a retrospective study of 16 cases Gupta, Monika
2010
203 2 p. 297-302
6 p.
artikel
40 Three rearrangements of chromosome 5 in a patient with myelodysplastic syndrome: an atypical deletion 5q, a complex intrachromosomal rearrangement of chromosome 5, and a paracentric inversion of chromosome 5 Douet-Guilbert, Nathalie
2010
203 2 p. 303-308
6 p.
artikel
41 Translocation (3;8)(q27;q24) in two cases of triple hit lymphoma Motlló, Cristina
2010
203 2 p. 328-332
5 p.
artikel
42 Trisomy 17 in congenital plexiform (multinodular) cellular schwannoma Tassano, Elisa
2010
203 2 p. 313-315
3 p.
artikel
43 Urine from current smokers induces centrosome aberrations and spindle defects in vitro in nonmalignant human cell lines Gabriel, Ute
2010
203 2 p. 253-262
10 p.
artikel
                             43 gevonden resultaten
 
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