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                             15 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Chromosomal aberrations in oral solitary fibrous tumor Manor, Esther
2007
174 2 p. 170-172
3 p.
artikel
2 Complete cytogenetic and molecular response after imatinib treatment for chronic myeloid leukemia in a patient with atypical karyotype and BCR-ABL b2a3 transcript Pienkowska-Grela, Barbara
2007
174 2 p. 111-115
5 p.
artikel
3 Complex karyotypes confer a poor survival in adult acute myeloid leukemia with unfavorable cytogenetic abnormalities Chen, Chih-Cheng
2007
174 2 p. 138-146
9 p.
artikel
4 Cryptic ins(4;11)(q21;q23q23) detected by fluorescence in situ hybridization: a variant of t(4;11)(q21;q23) in an infant with a precursor B-cell acute lymphoblastic leukemia report of a second case Tirado, C.A.
2007
174 2 p. 166-169
4 p.
artikel
5 Editorial board 2007
174 2 p. IFC-
1 p.
artikel
6 High-resolution analysis of 3p deletion in neuroblastoma and differential methylation of the SEMA3B tumor suppressor gene Nair, Prakash N.
2007
174 2 p. 100-110
11 p.
artikel
7 “Home-brew” FISH assay shows higher efficiency than BCR-ABL dual color, dual fusion probe in detecting microdeletions and complex rearrangements associated with t(9;22) in chronic myeloid leukemia Albano, Francesco
2007
174 2 p. 121-126
6 p.
artikel
8 Interphase fluorescence in situ hybridization in multiple myeloma and monoclonal gammopathy of undetermined significance without and with positive plasma cell identification: analysis of 192 cases from the Region of Southern Denmark Christensen, Jacob H.
2007
174 2 p. 89-99
11 p.
artikel
9 Isodicentric Philadelphia chromosomes in imatinib mesylate (Gleevec)-resistant patients Szych, Christine M.
2007
174 2 p. 132-137
6 p.
artikel
10 Lymphoplasmacytic lymphoma/Waldenström macroglobulinemia with inv(16)(p13q22) as a sole genetic abnormality Frater, John L.
2007
174 2 p. 161-165
5 p.
artikel
11 MLL amplification in acute myeloid leukemia Pajuelo-Gámez, Juan C.
2007
174 2 p. 127-131
5 p.
artikel
12 Physical mapping of distinct 7q22 deletions in uterine leiomyoma and analysis of a recently annotated 7q22 candidate gene Ptacek, T.
2007
174 2 p. 116-120
5 p.
artikel
13 13q deletions in B-cell lymphoproliferative disorders: frequent association with translocation Struski, Stephanie
2007
174 2 p. 151-160
10 p.
artikel
14 Table of contents 2007
174 2 p. A1-A2
nvt p.
artikel
15 Trisomy 7 in postoperative spindle cell nodules Micci, Francesca
2007
174 2 p. 147-150
4 p.
artikel
                             15 gevonden resultaten
 
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