threonine has been researched along with Dental Enamel Hypoplasia 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 | 2 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ahn, BD; Kim, JW; Kim, YJ; Lee, SH; Lee, SJ; Lee, SK; Lee, ZH | 1 |
Hu, JC; Mornet, E; Plaetke, R; Simmer, JP; Sun, X; Thomas, HF; Zhang, C | 1 |
2 other study(ies) available for threonine and Dental Enamel Hypoplasia
Article | Year |
---|---|
DLX3 mutation in a new family and its phenotypic variations.
Topics: Amelogenesis Imperfecta; Child; Codon; Cysteine; Dental Enamel Hypoplasia; Dental Pulp Cavity; Frameshift Mutation; Hair; Homeodomain Proteins; Humans; Male; Nails, Malformed; Pedigree; Phenotype; Sequence Deletion; Syndrome; Threonine; Transcription Factors | 2008 |
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 |