bromodeoxyuridine has been researched along with Klinefelter Syndrome in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Meer, B; Schempp, W | 1 |
| Fonatsch, C; Froster-Iskenius, U; Schwinger, E; Weigert, M | 1 |
| Drogue, M; Fraisse, J; Freycon, F; Lauras, B | 1 |
| Croce, CM; Knowles, BB; Koprowski, H | 1 |
4 other study(ies) available for bromodeoxyuridine and Klinefelter Syndrome
| Article | Year |
|---|---|
Cytologic evidence for three human X-chromosomal segments escaping inactivation.
Topics: Bromodeoxyuridine; DNA Replication; Female; Humans; Karyotyping; Klinefelter Syndrome; Lymphocytes; Male; Sex Chromosomes; X Chromosome; Y Chromosome | 1983 |
Replication pattern in XXY cells with fra(X).
Topics: Adolescent; Bromodeoxyuridine; Chromosome Fragility; Female; Humans; Intellectual Disability; Klinefelter Syndrome; Lymphocytes; Male; Metaphase; Sex Chromosomes; X Chromosome | 1982 |
[XXXX Y syndrome. Two new observations with anomalous origin of the left coronary artery in one case (author's transl)].
Topics: Adolescent; Bromodeoxyuridine; Child, Preschool; Coronary Vessel Anomalies; Dermatoglyphics; Humans; Karyotyping; Klinefelter Syndrome; Male; Radiography | 1979 |
Preferential retention of the human chromosome C-7 in human-(thymidine kinase deficient) mouse hybrid cells.
Topics: Animals; Azaguanine; Bromodeoxyuridine; Cell Line; Cell Transformation, Neoplastic; Chromosome Aberrations; Chromosome Disorders; Chromosomes; Chromosomes, Human, 6-12 and X; Clone Cells; Crosses, Genetic; Drug Resistance; Fibroblasts; Guanine; Humans; Hybrid Cells; Hypoxanthines; Karyotyping; Klinefelter Syndrome; Lesch-Nyhan Syndrome; Male; Mice; Mutation; Pentosyltransferases; Simian virus 40; Skin; Thymidine Kinase | 1973 |