cystine has been researched along with Autosomal Chromosome Disorders in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (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 |
---|---|
Becker, FL; Francke, U; Hammond, DS; Pellett, OL; Schneider, JA | 1 |
Kroll, W; Lichte, KH | 1 |
Nakagawa, H; Sato, T; Tada, K; Yokoyama, Y; Yoshida, T | 1 |
1 review(s) available for cystine and Autosomal Chromosome Disorders
Article | Year |
---|---|
Cystinosis: a review of the different forms and of recent advances.
Topics: Adult; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Cystine; Cystinosis; Diet Therapy; Dithiothreitol; Fanconi Syndrome; Fibroblasts; Heterozygote; Humans; Hybrid Cells; Infant; Kidney Transplantation; Lymphocytes; Pedigree; Prenatal Diagnosis; Syndrome; Transplantation, Homologous | 1973 |
2 other study(ies) available for cystine and Autosomal Chromosome Disorders
Article | Year |
---|---|
Properties of cystinotic fibroblast-D98 cell hybrids studied by somatic cell hybridization.
Topics: Cell Line; Child; Chromosome Aberrations; Chromosome Disorders; Chromosomes; Clone Cells; Cystine; Cystinosis; Fanconi Syndrome; Female; Fibroblasts; Glucosephosphate Dehydrogenase; Humans; Hybrid Cells; Hypoxanthines; Isoenzymes; Karyotyping; Syndrome | 1973 |
Cystathioninuria not associated with vitamin B6 dependency: a probably new type of cystathioninuria.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Autoanalysis; Carbon Isotopes; Child; Child, Preschool; Chromatography, Thin Layer; Chromosome Aberrations; Chromosome Disorders; Cystine; Electroencephalography; Humans; Infant; Liver; Liver Function Tests; Male; Methionine; Pyridoxine; Riboflavin; Serine; Sulfates | 1968 |