nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Acquired monosomy 7 in donor cells in a patient treated for acute lymphoblastic leukemia with bone marrow transplantation
|
Shekhter-Levin, Sofia |
|
1997 |
95 |
2 |
p. 190-197 8 p. |
artikel |
2 |
A new case of trisomy 21 in a patient with an acute nonlymphocytic leukemia (M5b)
|
Gallego, Marta |
|
1997 |
95 |
2 |
p. 213-214 2 p. |
artikel |
3 |
Announcement
|
|
|
1997 |
95 |
2 |
p. i- 1 p. |
artikel |
4 |
Association of hereditary angioedema and hereditary breast cancer
|
Christie, David R.H. |
|
1997 |
95 |
2 |
p. 159-162 4 p. |
artikel |
5 |
Chromosomal aberration in lipoblastoma: A case with 46,XX,ins(8;6)(q11.2;q13q27)
|
Kanazawa, Chikako |
|
1997 |
95 |
2 |
p. 163-165 3 p. |
artikel |
6 |
Clinical correlations of immunophenotypic variations and the presence of trisomy 12 in B-cell chronic lymphocytic leukemia
|
Tefferi, Ayalew |
|
1997 |
95 |
2 |
p. 173-177 5 p. |
artikel |
7 |
c-myc Amplification in a preleukemia patient with trisomy 4 and double minutes: Review of the unique coexistence of these two chromosome abnormalities in acute myelogenous leukemia
|
Reddy, Kavita S. |
|
1997 |
95 |
2 |
p. 206-209 4 p. |
artikel |
8 |
Cytogenetic and molecular genetic analysis of a pediatric pleomorphic sarcoma reveals similarities to adult malignant fibrous histiocytoma
|
Palmer, Jessica L. |
|
1997 |
95 |
2 |
p. 141-147 7 p. |
artikel |
9 |
Cytogenetic and molecular studies of siblings with ataxia telangiectasia followed for 7 years
|
Renedo, M. |
|
1997 |
95 |
2 |
p. 178-182 5 p. |
artikel |
10 |
Genetic aberrations in pediatric acute lymphoblastic leukemia by comparative genomic hybridization
|
Karhu, Ritva |
|
1997 |
95 |
2 |
p. 123-129 7 p. |
artikel |
11 |
Homozygous deletion of the neurofibromatosis-1 gene in the tumor of a patient with neuroblastoma
|
Martinsson, Tommy |
|
1997 |
95 |
2 |
p. 183-189 7 p. |
artikel |
12 |
Identification of chromosome changes in acute myeloid leukemia (AML-M2) by molecular cytogenetics
|
La Starza, Roberta |
|
1997 |
95 |
2 |
p. 148-152 5 p. |
artikel |
13 |
Molecular characterization of a complex chromosomal rearrangement in a pleomorphic salivary gland adenoma involving the 3′-UTR of HMGIC
|
Geurts, Jan M.W. |
|
1997 |
95 |
2 |
p. 198-205 8 p. |
artikel |
14 |
Myelodysplastic syndrome presenting with clonal rearrangement isolated to chromosomal region 1q
|
Mogul, Mark J. |
|
1997 |
95 |
2 |
p. 210-212 3 p. |
artikel |
15 |
Telomeric fusions in cultured human fibroblasts as a source of genomic instability
|
Riboni, Roberta |
|
1997 |
95 |
2 |
p. 130-136 7 p. |
artikel |
16 |
The expression of common fragile sites and genetic predisposition to squamous cell lung cancers
|
Egeli, Ünal |
|
1997 |
95 |
2 |
p. 153-158 6 p. |
artikel |
17 |
tHigh frequency of telomeric associations in human ovarian surface epithelial cells transformed by human papilloma viral oncogenes
|
Wan, Thomas S.K. |
|
1997 |
95 |
2 |
p. 166-172 7 p. |
artikel |
18 |
Two unbalanced translocations, t(12;22)(p13;q11) and t(12;?)(p13;?), in an aggressive chronic b-cell leukemia: TEL gene analysis using FISH
|
Conchon, Monika |
|
1997 |
95 |
2 |
p. 137-140 4 p. |
artikel |