| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An Update on DNA-Based BRCA1/BRCA2 Genetic Counseling in Hereditary Breast Cancer
|
Lynch, Henry T
|
|
1999
|
109 |
2 |
p. 91-98
8 p.
|
artikel
|
| 2 |
Correspondence
|
|
|
1999
|
109 |
2 |
p. 178-179
2 p.
|
artikel
|
| 3 |
Cumulation of TP53 Mutations and p16 INK4A /p15 INK4B Homozygous Deletions in Human Papilloma Virus Type 16 Positive Scrotal Cancer
|
Güran, Sxefik
|
|
1999
|
109 |
2 |
p. 108-113
6 p.
|
artikel
|
| 4 |
Cytogenetic Study of a Spindle-Cell Rhabdomyosarcoma of the Parotid Gland
|
Gil-Benso, Rosario
|
|
1999
|
109 |
2 |
p. 150-153
4 p.
|
artikel
|
| 5 |
Detection of Monosomy 7 in Bone Marrow by Fluorescence In Situ Hybridization
|
Thurston, Virginia C
|
|
1999
|
109 |
2 |
p. 154-160
7 p.
|
artikel
|
| 6 |
Development of Acute Promyelocytic Leukemia with Isochromosome 17q after BCR/ABL Positive Chronic Myeloid Leukemia
|
Ören, Hale
|
|
1999
|
109 |
2 |
p. 141-143
3 p.
|
artikel
|
| 7 |
Effect of Conditioned Medium, Nutritive Elements and Mitotic Synchronization on the Accuracy of the Cytogenetic Analysis in Patients with Chronic Myeloid Leukemia at Diagnosis and During α-Interferon Therapy
|
Castagné, C
|
|
1999
|
109 |
2 |
p. 166-171
6 p.
|
artikel
|
| 8 |
Embryonal Rhabdomyosarcoma with Only Numerical Chromosome Changes
|
Polito, Pietro
|
|
1999
|
109 |
2 |
p. 161-165
5 p.
|
artikel
|
| 9 |
Fluorescence In Situ Hybridization Analysis Shows the Frequent Occurrence of 14q32.3 Rearrangements with Involvement of Immunoglobulin Switch Regions in Myeloma Cell Lines
|
Kuipers, Jeroen
|
|
1999
|
109 |
2 |
p. 99-107
9 p.
|
artikel
|
| 10 |
Involvement of Chromosome Losses in the Progression and Metastasis Formation of a Human Malignant Melanoma
|
Balázs, Margit
|
|
1999
|
109 |
2 |
p. 114-118
5 p.
|
artikel
|
| 11 |
Isochromosome (12p) and Peritriploidy in a Highly Malignant Extrarenal Rhabdoid Tumor
|
Comtesse, P.P.F.Grandjean Perrenod
|
|
1999
|
109 |
2 |
p. 175-177
3 p.
|
artikel
|
| 12 |
Jumping Translocations Involving Chromosome 1q in a Patient with Crohn Disease and Acute Monocytic Leukemia
|
Reddy, K.S
|
|
1999
|
109 |
2 |
p. 144-149
6 p.
|
artikel
|
| 13 |
MYC Amplification in Two Further Cases of Acute Myeloid Leukemia with Trisomy 4 and Double Minute Chromosomes
|
O’Malley, Fran
|
|
1999
|
109 |
2 |
p. 123-125
3 p.
|
artikel
|
| 14 |
Neuroblastoma in Two Siblings Supports the Role of 1p36 Deletion in Tumor Development
|
Cunsolo, Crocifissa Lo
|
|
1999
|
109 |
2 |
p. 126-130
5 p.
|
artikel
|
| 15 |
PHA/IL2
|
Morgan, Rodman
|
|
1999
|
109 |
2 |
p. 134-137
4 p.
|
artikel
|
| 16 |
Premature Centromere Division in Patients with Multiple Endocrine Neoplasia Type 1
|
Sakurai, Akihiro
|
|
1999
|
109 |
2 |
p. 138-140
3 p.
|
artikel
|
| 17 |
Ring Chromosomes in a Malignant Mesenchymoma
|
van Kessel, A.Geurts
|
|
1999
|
109 |
2 |
p. 119-122
4 p.
|
artikel
|
| 18 |
Trisomy 22 in Acute Myeloid Leukemia
|
Wong, K.F
|
|
1999
|
109 |
2 |
p. 131-133
3 p.
|
artikel
|
| 19 |
Tumor Necrosis Factor Microsatellite Polymorphisms in Italian Glioblastoma Patients
|
Frigerio, S
|
|
1999
|
109 |
2 |
p. 172-174
3 p.
|
artikel
|
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