| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A corrected karyotype for the SH-SY5Y human neuroblastoma cell line
|
Spengler, Barbara A.
|
|
2002
|
138 |
2 |
p. 177-178
2 p.
|
artikel
|
| 2 |
Analysis of BRCA1, TP53, and TSG101 germline mutations in German breast and/or ovarian cancer families
|
Balz, Vera
|
|
2002
|
138 |
2 |
p. 120-127
8 p.
|
artikel
|
| 3 |
Atypical t(15;17)(q13;q12) in a patient with all-trans retinoic acid refractory secondary acute promyelocytic leukemia:
|
Kurian, Sobha
|
|
2002
|
138 |
2 |
p. 143-148
6 p.
|
artikel
|
| 4 |
Characterization of chromosomal aberrations in a case of glioblastoma multiforme combining cytogenetic and molecular cytogenetic techniques
|
Zuber, M.A.
|
|
2002
|
138 |
2 |
p. 111-115
5 p.
|
artikel
|
| 5 |
Chronic myelocytic leukemia with eosinophilia, t(9;12)(q34;p13), and ETV6-ABL gene rearrangement
|
Keung, Yi-Kong
|
|
2002
|
138 |
2 |
p. 139-142
4 p.
|
artikel
|
| 6 |
Complex cytogenetic abnormalities including telomeric associations and MEN1 mutation in a pediatric ependymoma
|
Urioste, M.
|
|
2002
|
138 |
2 |
p. 107-110
4 p.
|
artikel
|
| 7 |
Cryptic translocation of PML/RARA on 17q. A rare event in acute promyelocytic leukemia
|
Zaccaria, Alfonso
|
|
2002
|
138 |
2 |
p. 169-173
5 p.
|
artikel
|
| 8 |
Cryptic t(X;18), ins(6;18), and SYT-SSX2 gene fusion in a case of intraneural monophasic synovial sarcoma
|
Lestou, Valia S.
|
|
2002
|
138 |
2 |
p. 153-156
4 p.
|
artikel
|
| 9 |
Expression of the HMGA2-LPP fusion transcript in only 1 of 61 karyotypically normal pulmonary chondroid hamartomas
|
Lemke, Inga
|
|
2002
|
138 |
2 |
p. 160-164
5 p.
|
artikel
|
| 10 |
Frequency of 657del(5) mutation of the NBS1 gene in the Czech population by polymerase chain reaction with sequence specific primers
|
Drábek, Jir̆ı́
|
|
2002
|
138 |
2 |
p. 157-159
3 p.
|
artikel
|
| 11 |
Identification of t(15;17) and a segmental duplication of chromosome 11q23 in a patient with acute myeloblastic leukemia M2
|
Li, Shibo
|
|
2002
|
138 |
2 |
p. 149-152
4 p.
|
artikel
|
| 12 |
Involvement of 1p36 region in two cases of adenocarcinoma of the ampulla of Vater
|
Bernasconi, Barbara
|
|
2002
|
138 |
2 |
p. 133-138
6 p.
|
artikel
|
| 13 |
Molecular cytogenetic aberrations in CD30+ anaplastic large cell lymphoma cell lines
|
Gogusev, Jean
|
|
2002
|
138 |
2 |
p. 95-101
7 p.
|
artikel
|
| 14 |
Recurring breakpoints of 1p13∼p22 in osteochondroma
|
Sawyer, Jeffrey R.
|
|
2002
|
138 |
2 |
p. 102-106
5 p.
|
artikel
|
| 15 |
Sensitivity of detection of B-cell lymphoma in bone marrow by fluorescence in situ hybridization
|
Juenger, Christopher
|
|
2002
|
138 |
2 |
p. 174-176
3 p.
|
artikel
|
| 16 |
SKY detection of chromosome rearrangements in two cases of tMDS with a complex karyotype
|
Cohen, Ninette
|
|
2002
|
138 |
2 |
p. 128-132
5 p.
|
artikel
|
| 17 |
Trisomy 21 as the only recurrent chromosomal anomaly in a clinically aggressive ovarian carcinoma
|
Faruqi, Shamim A.
|
|
2002
|
138 |
2 |
p. 165-168
4 p.
|
artikel
|
| 18 |
Trisomy 15 in a case of pediatric hemangiopericytoma and review of the literature
|
Vadlamani, Indira
|
|
2002
|
138 |
2 |
p. 116-119
4 p.
|
artikel
|
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