| scholarly article | Q13442814 |
| P2093 | author name string | A. E. Retief | |
| W. A. van Niekerk | |||
| M. F. van der Riet-Fox | |||
| P2860 | cites work | Cancer Research | Q326097 |
| Acta Cytologica | Q15755265 | ||
| Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining | Q29614339 | ||
| Abnormalities of chromosome 1 in myeloproliferative disorders | Q33341792 | ||
| Distinct haematological disorder with deletion of long arm of no. 5 chromosome | Q34209827 | ||
| Mapping of human chromosomal regions related to neoplasia: Evidence from chromosomes 1 and 17 | Q35054247 | ||
| Nonrandom chromosomal abnormalities in hematologic disorders of man | Q35066603 | ||
| Chromosomal Abnormalities and Their Specificity in Human Neoplasms: An Assessment of Recent Observations by Banding Techniques | Q39620183 | ||
| Chromosomes and causation of human cancer and leukemia.XXVI. Banding studies in acute lymphoblastic leukemia (ALL) | Q40500238 | ||
| Duplication of part of the long arm of chromosome 1 in myelofibrosis terminating in acute myeloblasts leukemia | Q40529660 | ||
| Characterization of an established cell line (SH-3) derived from pleural effusion of patient with breast cancer | Q42803907 | ||
| Two pseudodiploid human breast carcinomas studied with G-band technique | Q45016837 | ||
| Isochromosome 17 in Prostatic Cancer | Q45242801 | ||
| Chromosomes 1 in 14 ovarian cancers. Heterochromatin variants and structural changes | Q46226642 | ||
| Abnormalities of chromosome No. 1 in human solid malignant tumours | Q46929735 | ||
| Chromosome analyses of a metastatic gastric carcinoma including quinacrine fluorescence | Q54325614 | ||
| 15/17 translocation, a consistent chromosomal change in acute promyelocytic leukaemia | Q66694390 | ||
| Chromosome 1 in cervical carcinoma | Q66696683 | ||
| Duplication of part of chromosome no. 1 in myeloproliferative diseases | Q66697507 | ||
| Chromosomes and causation of human cancer and leukemia. XVI. Banding studies of chronic myelocytic leukemia, including five unusual Ph11 translocations | Q66845440 | ||
| Chromosomes and causation of human cancer and leukemia. XI. Correlation of karyotypes with clinical features of acute myeloblastic leukemia | Q66849978 | ||
| Non-random chromosome changes in acute myeloid leukemia. Chromosome banding examination of 30 cases at diagnosis | Q66854846 | ||
| Clustering of aberrations to specific chromosomes in human neoplasms. II. A survey of 287 neoplasms | Q66854850 | ||
| Have double minutes functioning centromeres? | Q67327702 | ||
| Chromosomes and causation of human cancer and leukemia. X. Banding patterns in cancerous effusions | Q67338150 | ||
| Chromosomes and causation of human cancer and leukemia. XIV. Origin of a large number of markers in a cancer | Q67438174 | ||
| Trisomy of the Long Arm of Chromosome #1 in Human Leukemia | Q67440161 | ||
| Chromosomes and causation of human cancer and leukemia. XX. Banding patterns of primary tumors | Q67542465 | ||
| Chromosomes and causation of human cancer and leukemia. XXII. Karyotypic changes in malignant melanoma | Q67674153 | ||
| Characteristic chromosomal abnormalities in biopsies and lymphoid-cell lines from patients with Burkitt and non-Burkitt lymphomas | Q67770720 | ||
| The chromosomes and causation of human cancer and leukemia. XIX. Common markers in various tumors | Q67831184 | ||
| Human breast carcinomas: marker chromosomes involving 1q in seven cases | Q68209700 | ||
| Tumor etiology and chromosome pattern | Q68643032 | ||
| Chromosome banding pattern in human colonic polyps | Q68871287 | ||
| Identification of normal and abnormal chromosomes in tumor cells | Q69527604 | ||
| Differential binding of alkylating fluorochromes in human chromosomes | Q71442570 | ||
| A simple technique for demonstrating centromeric heterochromatin | Q93730570 | ||
| An analysis of the technical variables in the production of C bands | Q93735261 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | oncology | Q162555 |
| chromosome abnormality | Q744962 | ||
| P304 | page(s) | 2108-2119 | |
| P577 | publication date | 1979-12-01 | |
| P1433 | published in | Cancer | Q326041 |
| P1476 | title | Chromosome changes in 17 human neoplasms studied with banding | |
| P478 | volume | 44 |
| Q68343853 | A single chromosome rearrangement in one carcinoma of the cervix uteri |
| Q42089367 | Chromosomal imbalances in primary and metastatic pancreatic carcinoma as detected by interphase cytogenetics: basic findings and clinical aspects |
| Q68502493 | Chromosome 1 abnormalities in cervical carcinoma |
| Q67287194 | Chromosome abnormalities of gastric cancer detected in cancerous effusions |
| Q53386471 | Comparative genomic hybridization analysis detected frequent overrepresentation of chromosome 3q in squamous cell carcinoma of the lung. |
| Q54505710 | Complete or partial trisomy for the long arm of chromosome 1 in patients with various hematologic malignancies. |
| Q74036749 | Cytogenetic findings in thirty lung carcinoma patients |
| Q72405279 | Cytogenetics of small cell carcinoma of the lung |
| Q54563794 | Del(10)(q22.3q24.1) associated with juvenile polyposis. |
| Q73795023 | Duplication of 1q in a child with down syndrome and myelodysplastic syndrome |
| Q40960397 | Expression of FHIT in primary cultures of human epithelial ovarian tumors and malignant ovarian ascites. |
| Q36460450 | Genetic analysis of germ cell tumors: current progress and future prospects. |
| Q57250659 | Genetic epidemiology of epithelial ovarian cancer |
| Q74626484 | Isochromosome (12p) and peritriploidy in a highly malignant extrarenal rhabdoid tumor |
| Q35976936 | Karyotypic abnormalities in tumours of the pancreas |
| Q71010021 | Massive cytogenetic heterogeneity in a pancreatic carcinoma: fifty-four karyotypically unrelated clones |
| Q34255360 | Retinoblastoma: Clues to Human Oncogenesis |
| Q39651607 | Small metacentric marker chromosomes, particularly isochromosomes, in cancer |
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