Isochromosomes in neoplasia

Genes, Chromosomes and Cancer

Volumn 10, Issue 4, 1994, Pages 221-230

  Mertens, Fredrik ^a   Johansson, Bertil ^a   Mitelman, Felix ^a  

^a LUND UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADENOCARCINOMA; CHROMOSOME 12P; CHROMOSOME 17Q; CHROMOSOME 18Q; CHROMOSOME 1Q; CHROMOSOME 21Q; CHROMOSOME 5P; CHROMOSOME 6P; CHROMOSOME 7P; CHROMOSOME 9Q; CYTOGENETICS; HUMAN; ISOCHROMOSOME; MESOTHELIOMA; MYELODYSPLASTIC SYNDROME; NEOPLASM; PRIORITY JOURNAL; REVIEW; SARCOMA;

CHROMOSOME ABERRATIONS; HUMAN; NEOPLASMS; SUPPORT, NON-U.S. GOV'T;

EID: 0028075111     PISSN: 10452257     EISSN: 10982264     Source Type: Journal    
DOI: 10.1002/gcc.2870100402     Document Type: Review

References (55)

1. Chromosome changes in 43 carcinomas of the cervix uteri
2. 1‐negative leukemia: A clinical, cytogenetic, and molecular study
3. Isochromosome 17q in primitive neuroectodermal tumors of the central nervous system
4. Evidence for a 17p tumor related locus distinct from p53 in pediatric primitive neuroectodermal tumors
5. Isochromosome of chromosome 12: Clinically useful marker for male germ cell tumors
6. Examination of clonal variants from human malignant melanoma studied by chromosome banding analysis
7. Cyftogenetic studies on prolymphocytic leukemia. II. T cell prolymphocytic leukemia
8. TP53 tumor suppressor gene: A model for investigating human mutagenesis
9. How do human isochromosomes arise?
10. Misdivision and the genetics of the centromere
11. Deletions of interferon genes in acute lymphoblastic leukemia
12. Genetic alterations underlying colorectal tumorigenesis
13. p53 in chronic myelogenous leukemia in acute phase
14. p53 gene mutations in acute myeloid leukemia with 17p monosomy
15. GCSF gene is expressed but not rearranged in a patient with isochromosome 17q positive acute nonlymphocytic leukemia
16. A new type of chromosomal abnormality in gonadal dysgenesis
17. Structural evidence for the authenticity of the human retinoblastoma gene
18. Cytogenetic findings in a metastasizing primary testicular chondrosarcoma
19. A possible specific chromosome change in transitional cell carcinoma of the bladder
20. Isochromosome not translocation in trisomy 21q21q
21. p53 mutations in human cancers
22. Cytogenetic analysis of uveal melanoma. Consistent occurrence of monosomy 3 and trisomy 8q
23. Mechanism of i(6p) formation in retinoblastoma tumor cells
24. Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci
25. Mutations in the p53 gene in myelodysplastic syndromes
26. Synthesis of granulocyte colony‐stimulating factor and its requirement for terminal divisions in chronic myelogenous leukemia
27. Cytogenetic and immunohistochemical evidence for the germ cell origin of a subset of acute leukemias associated with mediastinal germ cell tumors
28. Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases
29. Identification of isochromosome 17 in myeloid leukemia
30. Nonrandom secondary chromosome aberrations in liposarcomas with t(12;16)
31. Molecular analysis of Philadelphia‐negative myeloproliferative syndromes with i(17q)
32. The Cytogenetic scenario of chronic myeloid leukemia
33. Identification of isochromosome 17 in acute myeloid leukaemia
34. Detection and analysis of origin of i(12p), a diagnostic marker of human male germ cell tumors, by fluoresecence in situ hybridization
35. p53 mutations in nonastrocytic human brain tumors
36. Gastric cancer with an i(8q) and long survival
37. Whole‐arm t(1;16) and i(1q) as sole abnormalities identify gain of 1q as a primary chromosomal abnormality in breast cancer
38. Chromosome aberrations and prognostic factors in therapy‐related myelodysplasia and acute nonlymphocytic leukemia
39. Isochromosome 1q as the sole karyotypic abnormality in a Sertoli cell tumor of the ovary
40. Prognostic significance of chromosome abnormalities in chronic lymphocytic leukaemia
41. Isochromosomes in childhood acute lymphoblastic leukemia: A collaborative study of 83 cases
42. Abnormalities of 2q: A common genetic link between rhabdomyosarcoma and hepatoblastoma?
43. Molecular cytogenetic analysis of i(12p)‐negative human male germ cell tumors
44. Infrequent p53 gene mutations in medulloblastomas
45. 1‐positive or ‐negative myeloid leukemia
46. Pericentromeric structure of human X “isochromosomes”: Evidence for molecular heterogeneity
47. Functional evidence for human tumour suppressor genes: Chromosome and molecular genetic studies
48. Identification of a recurring translocation site involving chromosome 6 in human malignant melanoma
49. Cytogenetic studies in 45 pediatric brain tumors
50. Chromosome analysis of 31 Wilms' tumors
51. Acute nonlymphocytic leukemia (AML) with isochromosome i(17q) as the sole chromosomal anomaly: A distinct entity?
52. Cytogenetic analysis of posterior uveal melanoma
53. Consistent chromosome abnormalities in squamous cell carcinoma of the vulva