lysine has been researched along with Autosomal Chromosome Disorders in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 18.7374 |
| 1990's | 1 (33.33) | 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 |
|---|---|
| Ezquieta Zubicaray, B; González Gancedo, P; Gracia Bouthelier, R; Iguacel, AO; Jariego Fente, CM; Varela Junquera, JM | 1 |
| Lichtenstein, JR; Martin, GR; McKusick, VA; Nigra, TP; Sussman, M | 1 |
| Dayras, JC; Lejeune, J; See, G | 1 |
3 other study(ies) available for lysine and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
[Gly380Arg and Asn540Lys mutations of fibroblast growth factor receptor 3 in achondroplasia and hypochndroplasia in the Spanish population].
Topics: Achondroplasia; Arginine; Asparagine; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 4; Genetic Counseling; Glycine; Humans; Lysine; Osteochondrodysplasias; Phenotype; Point Mutation; Protein-Tyrosine Kinases; Receptors, Fibroblast Growth Factor; RNA, Transfer, Amino Acid-Specific; Spain | 1999 |
Hydroxylysine-deficient skin collagen in a patient with a form of the Ehlers-Danlos syndrome.
Topics: Chromosome Aberrations; Chromosome Disorders; Collagen Diseases; Ehlers-Danlos Syndrome; Female; Fibroblasts; Genes, Recessive; Humans; Hydroxylysine; Ketoglutaric Acids; Lysine; Male; Middle Aged; Mixed Function Oxygenases; Pedigree; Procollagen-Proline Dioxygenase | 1974 |
[Cystinuria-lysinuria with dwarfism, facial dysmorphy, muscle hypoplasia and psychomotor retardation].
Topics: Abnormalities, Multiple; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Consanguinity; Cystinuria; Dwarfism; Face; Female; Humans; Infant; Karyotyping; Lysine; Muscular Diseases; Pedigree; Psychomotor Disorders | 1970 |