nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Association of genetic variants with pancreatic cancer
|
Skudra, Silvija |
|
2007 |
179 |
1 |
p. 76-78 3 p. |
artikel |
2 |
Automated JAK2V617F quantification using a magnetic filtration system and sequence-specific primer-single molecule fluorescence detection
|
Ohyashiki, Kazuma |
|
2007 |
179 |
1 |
p. 19-24 6 p. |
artikel |
3 |
Chronic myeloid leukemia with a rare variant BCR-ABL translocation: t(9;22;21)(q34;q11.2;q11.2)
|
Takeuchi, Mai |
|
2007 |
179 |
1 |
p. 85-87 3 p. |
artikel |
4 |
Clastogenic factors in the plasma of patients with hepatitis C: their possible role at the origin of hepatocarcinoma
|
Emerit, Ingrid |
|
2007 |
179 |
1 |
p. 31-35 5 p. |
artikel |
5 |
Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies
|
Maserati, Emanuela |
|
2007 |
179 |
1 |
p. 79-81 3 p. |
artikel |
6 |
Derivative (3)t(3;18)(q27;q21)t(18;16)(q21;?) involving the BCL2 and BCL6 genes in follicular lymphoma with t(3;14;18)(q27;q32;q21)
|
Yamamoto, Katsuya |
|
2007 |
179 |
1 |
p. 69-75 7 p. |
artikel |
7 |
Distinct structural abnormalities of chromosomes 11 and 12 associated with loss of heterozygosity in X-ray–induced mouse thymic lymphomas
|
Yoshida, Mitsuaki A. |
|
2007 |
179 |
1 |
p. 1-10 10 p. |
artikel |
8 |
Editorial board
|
|
|
2007 |
179 |
1 |
p. IFC- 1 p. |
artikel |
9 |
Gain of multiple copies of the CBFB gene: a new genetic aberration in a case of granulocytic sarcoma
|
Mallo, Mar |
|
2007 |
179 |
1 |
p. 62-65 4 p. |
artikel |
10 |
Identification of cryptic microaberrations in osteosarcoma by high-definition oligonucleotide array comparative genomic hybridization
|
Selvarajah, Shamini |
|
2007 |
179 |
1 |
p. 52-61 10 p. |
artikel |
11 |
Interrelationships among chromosome aneuploidy, promoter hypermethylation, and protein expression of the CDKN2A gene in individuals from northern Brazil with gastric adenocarcinoma
|
Guimarães, Adriana Costa |
|
2007 |
179 |
1 |
p. 45-51 7 p. |
artikel |
12 |
Inverted and deleted chromosome 16 with deletion of 3′ CBFB identified by fluorescence in situ hybridization
|
Spencer, Deborah V. |
|
2007 |
179 |
1 |
p. 82-84 3 p. |
artikel |
13 |
Isochromosome (X)(p10) in hematologic disorders: FISH study of 14 new cases show three types of centromere signal patterns
|
Adeyinka, Adewale |
|
2007 |
179 |
1 |
p. 25-30 6 p. |
artikel |
14 |
Mapping of constitutional translocation breakpoints in renal cell cancer patients: identification of KCNIP4 as a candidate gene
|
Bonne, Anita |
|
2007 |
179 |
1 |
p. 11-18 8 p. |
artikel |
15 |
p53 pathway gene single nucleotide polymorphisms and chronic lymphocytic leukemia
|
Lahiri, Onoshua |
|
2007 |
179 |
1 |
p. 36-44 9 p. |
artikel |
16 |
Premature chromatid separation in a woman with carcinoma in situ of the uterine cervix and in her son with keratoacanthoma
|
Petković, Iskra |
|
2007 |
179 |
1 |
p. 66-68 3 p. |
artikel |
17 |
Table of contents
|
|
|
2007 |
179 |
1 |
p. A1-A2 nvt p. |
artikel |