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                             20 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Acute myeloid leukemia (AML) with t(8;21)(q22;q22) relapsing as AML with t(3;21)(q26;q22) Bacher, Ulrike
2006
168 2 p. 172-174
3 p.
artikel
2 A new complex chromosomal translocation t(2;12;21)(q33;p13;q22) in B-cell acute lymphoblastic leukemia Vasquez-Jimenez, E.A.
2006
168 2 p. 179-180
2 p.
artikel
3 APC and CTNNB1 mutations are rare in sporadic ependymomas Onilude, Olabisi E.
2006
168 2 p. 158-161
4 p.
artikel
4 A translocation involving the placental growth factor gene is identified in an epithelioid hemangioendothelioma He, Mai
2006
168 2 p. 150-154
5 p.
artikel
5 Clinical, immunophenotypic, and molecular profiling of trisomy 12 in chronic lymphocytic leukemia and comparison with other karyotypic subgroups defined by cytogenetic analysis Athanasiadou, Anastasia
2006
168 2 p. 109-119
11 p.
artikel
6 COL1A1-PDGFB fusion in a pediatric Bednar tumor with 2 copies of a der(22)t(17;22) Craver, Randall
2006
168 2 p. 155-157
3 p.
artikel
7 Construction of evolutionary tree models for nasopharyngeal carcinoma using comparative genomic hybridization data Shih-Hsin Wu, Lawrence
2006
168 2 p. 105-108
4 p.
artikel
8 Cytogenetic studies of a series of 43 consecutive secondary myelodysplastic syndromes/acute myeloid leukemias: conventional cytogenetics, FISH, and multiplex FISH Shali, Wei
2006
168 2 p. 133-145
13 p.
artikel
9 Editorial board 2006
168 2 p. CO2-
1 p.
artikel
10 Genomic profiles of colorectal cancers differ based on patient smoking status Swede, Helen
2006
168 2 p. 98-104
7 p.
artikel
11 Identification of 13q deletion, trisomy 1q, and IgH rearrangement as the most frequent chromosomal changes found in Korean patients with multiple myeloma Bang, Soo-Mee
2006
168 2 p. 124-132
9 p.
artikel
12 Infant acute lymphoblastic leukemia with t(11;16)(q23;p13.3) and lineage switch into acute monoblastic leukemia Stasik, Christopher
2006
168 2 p. 146-149
4 p.
artikel
13 Isolated tetrasomy 13: a fifth case report of a rare chromosome abnormality associated with poorly differentiated acute myeloid leukemia Roche-Lestienne, Catherine
2006
168 2 p. 181-182
2 p.
artikel
14 Linking the human cytogenetic map with nucleotide sequence: the CCAP clone set Jang, Wonhee
2006
168 2 p. 89-97
9 p.
artikel
15 Low frequency of large genomic rearrangements of BRCA1 and BRCA2 in western Denmark Thomassen, Mads
2006
168 2 p. 168-171
4 p.
artikel
16 MLL–SEPT6 fusion transcript with a novel sequence in an infant with acute myeloid leukemia Kadkol, ShriHari S.
2006
168 2 p. 162-167
6 p.
artikel
17 Random aneuploidy in CML patients at diagnosis and under imatinib treatment Amiel, A.
2006
168 2 p. 120-123
4 p.
artikel
18 Simultaneous presence of t(10;11)(p12;q23) and t(11;19)(q23;p13.1) in an infantile acute myeloid leukemia Wu, Shi-Qi
2006
168 2 p. 175-176
2 p.
artikel
19 Table of contents 2006
168 2 p. A1-A2
nvt p.
artikel
20 Unexpected cytogenetic finding in acute lymphoblastic leukemia: a case of del(5q) with a cryptic t(12;21) South, Sarah T.
2006
168 2 p. 177-178
2 p.
artikel
                             20 gevonden resultaten
 
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