thymine has been researched along with A-Thalassemia in 2 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "A beta-thalassemia intermedia phenotype can be caused by multiple genotypes." | 1.30 | Double heterozygosity for the codon beta 39 C-to-T nonsense mutation and a triplicate alpha-globin gene locus can cause "dominantly" inherited beta-thalassemia intermedia. ( Files, JC; Harrell, A; Li, J; Plonczynski, M; Rhodes, SL; Safaya, S; Steinberg, MH, 1999) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (100.00) | 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 |
|---|---|
| Rhodes, SL | 1 |
| Plonczynski, M | 1 |
| Harrell, A | 1 |
| Li, J | 1 |
| Safaya, S | 1 |
| Files, JC | 1 |
| Steinberg, MH | 1 |
| Costa, FF | 1 |
| Figueredo, MS | 1 |
| Sonati, MF | 1 |
| Kimura, EM | 1 |
| Martins, CS | 1 |
2 other studies available for thymine and A-Thalassemia
| Article | Year |
|---|---|
Double heterozygosity for the codon beta 39 C-to-T nonsense mutation and a triplicate alpha-globin gene locus can cause "dominantly" inherited beta-thalassemia intermedia.
Topics: alpha-Thalassemia; beta-Thalassemia; Codon; Cytosine; Female; Globins; Heterozygote; Humans; Mutatio | 1999 |
The IVS-I-110 (G-->T) and codon 39 (C-->T) beta-thalassemia mutations in association with alpha-thal-2 (-3.7 Kb) and Hb Hasharon [alpha 47(CE5)Asp-->His] in a Brazilian patient.
Topics: alpha-Thalassemia; Base Sequence; beta-Thalassemia; Brazil; Codon; Cytosine; Female; Guanine; Hemogl | 1992 |