thymine has been researched along with Autosomal Hemophilia A in 2 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "DNA of 70 unrelated hemophilia B patients, including three inhibitor patients, was analyzed by using various restriction enzymes and was hybridized with both a factor IX cDNA and 3'- and 5'-flanking probes." | 1.28 | Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia B. ( Brackmann, HH; Egli, H; Eigel, A; Horst, J; Ludwig, M; Olek, K; Schwaab, R, 1989) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 1 (50.00) | 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 |
|---|---|
| Nafa, K | 1 |
| Baudis, M | 1 |
| Deburgrave, N | 1 |
| Bardin, JM | 1 |
| Sultan, Y | 1 |
| Kaplan, JC | 1 |
| Delpech, M | 1 |
| Ludwig, M | 1 |
| Schwaab, R | 1 |
| Eigel, A | 1 |
| Horst, J | 1 |
| Egli, H | 1 |
| Brackmann, HH | 1 |
| Olek, K | 1 |
2 other studies available for thymine and Autosomal Hemophilia A
| Article | Year |
|---|---|
A novel mutation (Arg-->Leu in exon 18) in factor VIII gene responsible for moderate hemophilia A.
Topics: Arginine; Base Sequence; Blotting, Southern; Codon; DNA; Exons; Factor VIII; Female; Guanine; Hemoph | 1992 |
Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia B.
Topics: Chromosome Deletion; Cytosine; DNA; Factor IX; Female; Genes; Hemophilia A; Humans; Male; Mutation; | 1989 |