fibrinogen has been researched along with Disomy, Uniparental in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ding, Q; Ouyang, Q; Shen, Y; Wang, H; Wang, X; Xi, X | 1 |
| Asselta, R; Duga, S; Mahasandana, C; Malcovati, M; Peyvandi, F; Spena, S; Tenchini, ML | 1 |
2 other study(ies) available for fibrinogen and Disomy, Uniparental
| Article | Year |
|---|---|
Maternal chromosome 4 heterodisomy/isodisomy and Bβ chain Trp323X mutation resulting in severe hypodysfibrinogenaemia.
Topics: Afibrinogenemia; Base Sequence; Child; Chromosomes, Human, Pair 4; Codon, Nonsense; DNA Mutational Analysis; Female; Fibrinogen; Homozygote; Humans; Male; Microsatellite Repeats; Pedigree; Uniparental Disomy | 2012 |
Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene.
Topics: Afibrinogenemia; Base Sequence; Chromosome Mapping; Chromosomes, Human, Pair 4; DNA Mutational Analysis; Female; Fibrinogen; Homozygote; Humans; Male; Microsatellite Repeats; Molecular Sequence Data; Pedigree; Point Mutation; Sequence Deletion; Uniparental Disomy | 2004 |