thymine has been researched along with Ichthyosis, Lamellar in 1 studies
Ichthyosis, Lamellar: A chronic, congenital ichthyosis inherited as an autosomal recessive trait. Infants are usually born encased in a collodion membrane which sheds within a few weeks. Scaling is generalized and marked with grayish-brown quadrilateral scales, adherent at their centers and free at the edges. In some cases, scales are so thick that they resemble armored plate.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (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 |
|---|---|
| Tok, J | 1 |
| Garzon, MC | 1 |
| Cserhalmi-Friedman, P | 1 |
| Lam, HM | 1 |
| Spitz, JL | 1 |
| Christiano, AM | 1 |
1 other study available for thymine and Ichthyosis, Lamellar
| Article | Year |
|---|---|
Identification of mutations in the transglutaminase 1 gene in lamellar ichthyosis.
Topics: Amino Acid Sequence; Amino Acid Substitution; Base Sequence; Diseases in Twins; Exons; Female; Guani | 1999 |