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                             19 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 An indolent B-cell lymphoma with t(2;8)(p12;q24) abnormality and absence of C-MYC amplification and TP53 deletion. A new variant? Potti, Anil
2003
144 1 p. 76-79
4 p.
artikel
2 Application of comparative genomic hybridization technique for detection of chromosomal aberrations in benign cystic teratoma Amiel, A.
2003
144 1 p. 73-75
3 p.
artikel
3 Arm-specific multicolor fluorescence in situ hybridization reveals widespread chromosomal instability in glioma cell lines Sallinen, Satu-Leena
2003
144 1 p. 52-60
9 p.
artikel
4 Array comparative genomic hybridization analysis of myelodysplastic syndromes with complex karyotypes. A technical evaluation Martı́nez-Ramı́rez, A.
2003
144 1 p. 87-89
3 p.
artikel
5 A xeno-transplantable plasma cell leukemia line with a split translocation of the IgH gene Ohbayashi, Kaneyuki
2003
144 1 p. 31-35
5 p.
artikel
6 Cancer Genetics and Cytogenetics 2003
144 1 p. IFC-
1 p.
artikel
7 Chromosomal gains and losses in ocular melanoma detected by comparative genomic hybridization in an Australian population-based study Vajdic, Claire M
2003
144 1 p. 12-17
6 p.
artikel
8 Cytogenetic characterization of three malignant peripheral nerve sheath tumors Frank, Derk
2003
144 1 p. 18-22
5 p.
artikel
9 Cytogenetic findings in a case of dedifferentiated chondrosarcoma Casorzo, Laura
2003
144 1 p. 61-64
4 p.
artikel
10 Cytogenetics, fluorescence in situ hybridization, and reverse transcriptase polymerase chain reaction are necessary to clarify the various mechanisms leading to an MLL-AF10 fusion in acute myelocytic leukemia with 10;11 rearrangement Klaus, Mirjam
2003
144 1 p. 36-43
8 p.
artikel
11 Deletion of chromosome 15 represents a rare but recurrent chromosomal abnormality in myelocytic malignancies Dierlamm, Judith
2003
144 1 p. 1-5
5 p.
artikel
12 Establishment of a new human malignant fibrous histiocytoma cell line, FU-MFH-1: cytogenetic characterization by comparative genomic hybridization and fluorescence in situ hybridization Nishio, Jun
2003
144 1 p. 44-51
8 p.
artikel
13 Evaluation of PARVG located on 22q13 as a candidate tumor suppressor gene for colorectal and breast cancer Castellvı́-Bel, Sergi
2003
144 1 p. 80-82
3 p.
artikel
14 Interphase cytogenetic characterization of aberrations in the long arm of chromosome 1 in B-cell lymphoid malignancies Weng, Lihong
2003
144 1 p. 83-84
2 p.
artikel
15 Loss of 1p and 7p in radiation-induced meningiomas identified by comparative genomic hybridization Rajcan-Separovic, Evica
2003
144 1 p. 6-11
6 p.
artikel
16 Monosomy 7p in meningiomas: a rare constituent of tumor progression Henn, Wolfram
2003
144 1 p. 65-68
4 p.
artikel
17 Tetrasomy 6 and 6q14 deletion are associated with better survival in hepatocellular carcinomas Huang, Shiu-Feng
2003
144 1 p. 23-30
8 p.
artikel
18 The common fragile site FRA16C does not map within the 16q smallest region of overlap number 2 frequently lost in breast carcinoma Taine, Laurence
2003
144 1 p. 85-86
2 p.
artikel
19 Trisomy 13 in a patient with common acute lymphoblastic leukemia: description of a case and review of the literature Spirito, Francesca R.
2003
144 1 p. 69-72
4 p.
artikel
                             19 gevonden resultaten
 
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