| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Banded chromosomes versus fluorescence in situ hybridization in the diagnosis of mantle cell lymphoma
|
Mohamed, Anwar N
|
|
2002
|
136 |
2 |
p. 108-112
5 p.
|
artikel
|
| 2 |
Comparative genomic hybridization detects specific cytogenetic abnormalities in pediatric ependymomas and choroid plexus papillomas
|
Grill, Jacques
|
|
2002
|
136 |
2 |
p. 121-125
5 p.
|
artikel
|
| 3 |
Fluorescence in situ hybridization for the study of cell lineage involvement in myelodysplastic syndromes with chromosome 5 anomalies
|
Anderson, Kristina
|
|
2002
|
136 |
2 |
p. 101-107
7 p.
|
artikel
|
| 4 |
High resolution analysis of chromosome 18 alterations in ulcerative colitis-related colorectal cancer
|
Terdiman, Jonathan P
|
|
2002
|
136 |
2 |
p. 129-137
9 p.
|
artikel
|
| 5 |
Losses in chromosomes 17, 19, and 22q in neurofibromatosis type 1 and sporadic neurofibromas
|
Koga, Takamasa
|
|
2002
|
136 |
2 |
p. 113-120
8 p.
|
artikel
|
| 6 |
Molecular cytogenetic analysis of clustered sporadic and familial renal cell carcinoma-associated 3q13∼q22 breakpoints
|
Bodmer, Daniëlle
|
|
2002
|
136 |
2 |
p. 95-100
6 p.
|
artikel
|
| 7 |
Molecular cytogenetic characterization of a complex rearrangement involving chromosomes 9 and 22 in a case of Ph-negative chronic myeloid leukemia
|
Storlazzi, Clelia Tiziana
|
|
2002
|
136 |
2 |
p. 141-145
5 p.
|
artikel
|
| 8 |
Mutations in the runt homology domain of CBFα2 in myeloid malignancies with acquired trisomy 21
|
Snaddon, Jennifer
|
|
2002
|
136 |
2 |
p. 151-152
2 p.
|
artikel
|
| 9 |
Myelodysplastic syndrome with transformation to AML-M7 in a 46,XX male patient
|
Lau, Lai-Ching
|
|
2002
|
136 |
2 |
p. 153-154
2 p.
|
artikel
|
| 10 |
Precursor T-lymphoblastic leukemia with a novel t(1;22)(p34;q13)
|
Wong, K.F
|
|
2002
|
136 |
2 |
p. 146-148
3 p.
|
artikel
|
| 11 |
Spontaneous clinical and cytogenetic remission of aplastic anemia in a patient with del(13q)
|
Saitoh, Takashi
|
|
2002
|
136 |
2 |
p. 126-128
3 p.
|
artikel
|
| 12 |
The BCR/ABL-extra signal fluorescence in situ hybridization system reliably detects deletions upstream of the ABL locus
|
Müller, Christel
|
|
2002
|
136 |
2 |
p. 149-150
2 p.
|
artikel
|
| 13 |
Transient myeloproliferative disorder in a phenotypically normal infant with i(21q) mosaicism
|
Wu, Shi-Qi
|
|
2002
|
136 |
2 |
p. 138-140
3 p.
|
artikel
|
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