scholarly article | Q13442814 |
review article | Q7318358 |
P356 | DOI | 10.1126/SCIENCE.6320372 |
P953 | full work available at URL | https://syndication.highwire.org/content/doi/10.1126/science.6320372 |
P698 | PubMed publication ID | 6320372 |
P2093 | author name string | W. F. Benedict | |
A. L. Murphree | |||
P2860 | cites work | Journal of the National Cancer Institute | Q400279 |
American Journal of Human Genetics | Q4744249 | ||
Chromosome number 11 and Wilms' tumor | Q72925909 | ||
Mutation and cancer: statistical study of retinoblastoma | Q24618185 | ||
Human-tumor-derived cell lines contain common and different transforming genes | Q34245850 | ||
T24 human bladder carcinoma oncogene is an activated form of the normal human homologue of BALB- and Harvey-MSV transforming genes | Q34253435 | ||
Cellular Transforming Genes | Q34253517 | ||
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma | Q34264957 | ||
N.A.S. symposium: new evidence as the basis for increased efforts in cancer research | Q34700414 | ||
A general theory of carcinogenesis | Q34744320 | ||
Genetics and the Etiology of Childhood Cancer | Q37019539 | ||
Cellular Oncogenes and Multistep Carcinogenesis | Q40161805 | ||
Second nonocular tumors in retinoblastoma survivors. Are they radiation-induced? | Q40229965 | ||
Chromosome 1 in 26 carcinomas of the cervix uteriStructural and numerical changes | Q40608870 | ||
Hereditary Renal-Cell Carcinoma Associated with a Chromosomal Translocation | Q41751694 | ||
Amplified DNA with limited homology to myc cellular oncogene is shared by human neuroblastoma cell lines and a neuroblastoma tumour | Q42799715 | ||
Correlation Between Balance of Specific Chromosomes and Expression of Malignancy in Hamster Cells 2 | Q44458293 | ||
Chromosome changes in 17 human neoplasms studied with banding | Q44683654 | ||
Chromosomes 1 in 14 ovarian cancers. Heterochromatin variants and structural changes | Q46226642 | ||
Abnormalities of chromosome No. 1 in human solid malignant tumours | Q46929735 | ||
Familial Retinoblastoma and Chromosome 13 Deletion Transmitted via an Insertional Translocation | Q53569910 | ||
The chromosomal basis of human neoplasia. | Q53762162 | ||
Nonrandom distribution of chromosomal aberrations induced by three chemicals. | Q54565358 | ||
Patient with 13 Chromosome Deletion: Evidence That the Retinoblastoma Gene Is a Recessive Cancer Gene | Q55062498 | ||
Multiple karyotypic changes in retinoblastoma tumor cells: Presence of normal chromosome No. 13 in most tumors | Q58348288 | ||
Human breast carcinomas: marker chromosomes involving 1q in seven cases | Q68209700 | ||
Renal Carcinoma (Hypernephroma) Occurring in 5 Siblings | Q69374279 | ||
Human cell hybrids: analysis of transformation and tumorigenicity | Q70264695 | ||
Familial renal cell carcinoma with a 3;11 chromosome translocation limited to tumor cells | Q70439023 | ||
Abnormalities of chromosome #13 in retinoblastomas from individuals with normal constitutional karyotypes | Q70448253 | ||
High rate of detection of 13q14 deletion mosaicism among retinoblastoma patients (using more extensive methods) | Q70480845 | ||
Similar chromosomal abnormalities in several retinoblastomas | Q70601008 | ||
Nonrandom chromosomal changes in untreated retinoblastomas | Q71139588 | ||
Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14 | Q71198008 | ||
Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase D | Q71656765 | ||
Specific chromosome defect associated with human small-cell lung cancer; deletion 3p(14-23) | Q72916321 | ||
P433 | issue | 4640 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | retinoblastoma | Q500695 |
Suppression, Genetic | Q71148826 | ||
P304 | page(s) | 1028-1033 | |
P577 | publication date | 1984-03-01 | |
1984-03-09 | |||
P1433 | published in | Science | Q192864 |
P1476 | title | Retinoblastoma: clues to human oncogenesis | |
Retinoblastoma: Clues to Human Oncogenesis | |||
P478 | volume | 223 |
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