threonine has been researched along with Diseases in Twins in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Haataja, R; Hallman, M; Löfgren, J; Marttila, R; Rämet, M | 1 |
Gross, C; Hehr, U; Martin, P; Schneider, S; Uyanik, G; Wiemer-Kruel, A; Winkler, J | 1 |
Hu, JC; Mornet, E; Plaetke, R; Simmer, JP; Sun, X; Thomas, HF; Zhang, C | 1 |
3 other study(ies) available for threonine and Diseases in Twins
Article | Year |
---|---|
Surfactant protein B polymorphism and respiratory distress syndrome in premature twins.
Topics: Diseases in Twins; Female; Gene Frequency; Genotype; Haplotypes; Humans; Infant, Newborn; Infant, Premature; Male; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Pulmonary Surfactants; Respiratory Distress Syndrome, Newborn; Retrospective Studies; Risk Factors; Threonine; Twins, Dizygotic; Twins, Monozygotic | 2003 |
Different clinical and morphological phenotypes in monozygotic twins with identical DCX mutation.
Topics: Alcohol Oxidoreductases; Cerebral Cortex; Child; Cysteine; Diagnosis, Differential; Diseases in Twins; DNA Mutational Analysis; Exons; Female; Humans; Magnetic Resonance Imaging; Mutation; Phenotype; Sugar Alcohol Dehydrogenases; Threonine; Twins, Monozygotic | 2004 |
Characterization of a family with dominant hypophosphatasia.
Topics: Alanine; Alkaline Phosphatase; Amino Acid Substitution; Child; Dental Cementum; Dental Enamel Hypoplasia; Diseases in Twins; Ethanolamines; Family Health; Female; Genes, Dominant; Genetic Linkage; Humans; Hypophosphatasia; Male; Pedigree; Point Mutation; Threonine; Tooth Exfoliation; Twins, Dizygotic | 2000 |