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 |