| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Chromosome Alterations in Renal Cell Carcinoma of Childhood May Correspond to Aberrations in Adults
|
Pedersen, Rikke K
|
|
1998
|
106 |
2 |
p. 166-169
4 p.
|
artikel
|
| 2 |
Clear-Cell and Papillary Carcinoma of the Kidney
|
Hughson, Michael D.
|
|
1998
|
106 |
2 |
p. 93-104
12 p.
|
artikel
|
| 3 |
Complex Structural Involvement of Chromosome 7 in Primary Myelodysplastic Syndromes Determined by Fluorescence In Situ Hybridization
|
Sessarego, Mario
|
|
1998
|
106 |
2 |
p. 110-115
6 p.
|
artikel
|
| 4 |
Correspondence
|
|
|
1998
|
106 |
2 |
p. 182-
1 p.
|
artikel
|
| 5 |
Detection of Chromosomal Aberrations in Tumor Cells and Tumor Infiltrating Lymphocytes by Molecular Cytogenetics in Patients with Gynecological Cancer
|
Engel, Heike
|
|
1998
|
106 |
2 |
p. 159-165
7 p.
|
artikel
|
| 6 |
Discrepant Cytogenetic and Fluorescence In Situ Hybridization Results in a 26-Year-Old Male with Early T-Cell Acute Lymphocytic Leukemia
|
Chinnappan, Dharmaraj
|
|
1998
|
106 |
2 |
p. 116-121
6 p.
|
artikel
|
| 7 |
Erratum
|
|
|
1998
|
106 |
2 |
p. 183-
1 p.
|
artikel
|
| 8 |
Evidence for Genetic Heterogeneity of the Carney Complex (Familial Atrial Myxoma Syndromes)
|
Milunsky, Jeff
|
|
1998
|
106 |
2 |
p. 173-176
4 p.
|
artikel
|
| 9 |
Fluorescence In Situ Hybridization Characterization of the Chromosomal Breakpoints in a Case with ins(17;3)(q11.2;q21q26.3) and Acute Monocytic Leukemia
|
Schnittger, Susanne
|
|
1998
|
106 |
2 |
p. 122-127
6 p.
|
artikel
|
| 10 |
Fluorescence In Situ Hybridization Studies of Interphase Nuclei for Assessing Response to Therapy in Patients with Chronic Myeloid Leukemia
|
Kobzev, Yuri
|
|
1998
|
106 |
2 |
p. 128-134
7 p.
|
artikel
|
| 11 |
Involvement of 3q21 in Nodular Fasciitis
|
Weibolt, Vines M
|
|
1998
|
106 |
2 |
p. 177-179
3 p.
|
artikel
|
| 12 |
Mononucleotide Repeat Instability Is Infrequent in Neuroblastoma
|
Hogarty, Michael D
|
|
1998
|
106 |
2 |
p. 140-143
4 p.
|
artikel
|
| 13 |
Novel Breakpoints of the EWS Gene and the WT1 Gene in a Desmoplastic Small Round Cell Tumor
|
Shimizu, Yukitoshi
|
|
1998
|
106 |
2 |
p. 156-158
3 p.
|
artikel
|
| 14 |
Polyploidy in Myelodysplastic Syndrome
|
Manley, R.
|
|
1998
|
106 |
2 |
p. 170-172
3 p.
|
artikel
|
| 15 |
Structural Alterations of Chromosome 5 in Twelve Human Prostate Cancer Cell Lines
|
Ozen, Mustafa
|
|
1998
|
106 |
2 |
p. 105-109
5 p.
|
artikel
|
| 16 |
Trisomy 6 and Double Minute Chromosomes in a Case of Chronic Myelomonocytic Leukemia
|
Sambani, Constantina
|
|
1998
|
106 |
2 |
p. 180-181
2 p.
|
artikel
|
| 17 |
Trisomy 14 and Leukemia
|
Reddy, K.S.
|
|
1998
|
106 |
2 |
p. 144-151
8 p.
|
artikel
|
| 18 |
Trisomy 6 as a Primary Karyotypic Aberration in Hematologic Disorders
|
Mohamed, Anwar N.
|
|
1998
|
106 |
2 |
p. 152-155
4 p.
|
artikel
|
| 19 |
Unusual Presentation of Multiple Myeloma with “Jumping Translocation” Involving 1q21
|
Keung, Yi-Kong
|
|
1998
|
106 |
2 |
p. 135-139
5 p.
|
artikel
|
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