tryptophan has been researched along with Abnormalities, Teeth in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (75.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cai, T; Dong, M; Duan, X; Gao, S; He, L; Hu, K; Li, Q; Mao, T; Shi, S; Wang, L; Xia, D; Xue, Y | 1 |
| Bailleul-Forestier, I; Bennaceur, S; de Roux, N; Gros, C; Leger, J; Zenaty, D | 1 |
| Duan, X; Mao, T; Wang, W; Xue, Y | 1 |
| Freire-Maia, N | 1 |
4 other study(ies) available for tryptophan and Abnormalities, Teeth
| Article | Year |
|---|---|
Dental Abnormalities Caused by Novel Compound Heterozygous CTSK Mutations.
Topics: Adenine; Adult; Alleles; Alveolar Process; Amino Acid Sequence; Animals; Cathepsin K; Chlorocebus aethiops; Codon, Terminator; Conserved Sequence; COS Cells; Cysteine; Dental Cementum; Guanine; Heterozygote; Humans; Male; Models, Genetic; Mutation, Missense; Pedigree; Phenol; Pycnodysostosis; Radiography, Panoramic; Tooth Abnormalities; Tryptophan; Tyrosine; X-Ray Microtomography | 2015 |
Dental agenesis in Kallmann syndrome individuals with FGFR1 mutations.
Topics: Adenine; Adolescent; Adult; Anodontia; Arginine; Bicuspid; Child, Preschool; Cleft Palate; Cysteine; Cytosine; Female; Glutamine; Glycine; Guanine; Humans; Incisor; Kallmann Syndrome; Male; Middle Aged; Molar; Mutation; Receptor, Fibroblast Growth Factor, Type 1; Sequence Deletion; Tooth Abnormalities; Tooth Root; Tooth, Deciduous; Tryptophan; Young Adult | 2010 |
Report of two Chinese patients suffering from CLCN7-related osteopetrosis and root dysplasia.
Topics: Adult; Arginine; Bone Density; China; Chloride Channels; Dentofacial Deformities; Genes, Recessive; Genetic Variation; Heterozygote; Homozygote; Humans; Leucine; Male; Osteomyelitis; Osteopetrosis; Osteosclerosis; Phenotype; Point Mutation; Proline; Tooth Abnormalities; Tooth Root; Tooth, Unerupted; Tryptophan | 2012 |
A newly recognized genetic syndrome of tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities.
Topics: Abnormalities, Multiple; Adolescent; Adult; Alopecia; Animals; Brazil; Breast; Child; Cleft Lip; Cleft Palate; Ear Deformities, Acquired; Ectodermal Dysplasia; Ectromelia; Electrocardiography; Electroencephalography; Growth Disorders; Heart Function Tests; Humans; Hypogonadism; Infant, Newborn; Intellectual Disability; Limb Deformities, Congenital; Male; Pedigree; Sibling Relations; Skin Abnormalities; Thyroid Gland; Tooth Abnormalities; Tryptophan | 1970 |