trolamine salicylate has been researched along with Noonan Syndrome in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Chen, L; Dong, Z; Lu, W; Ma, X; Ni, J; Shi, J; Wang, D; Wang, J; Wang, W; Xiao, Y; Yang, L; Zhang, C | 1 |
1 other study(ies) available for trolamine salicylate and Noonan Syndrome
Article | Year |
---|---|
Pathogenic gene screening in 91 Chinese patients with short stature of unknown etiology with a targeted next-generation sequencing panel.
Topics: Adolescent; Aggrecans; Arthritis; Asian People; Cartilage Oligomeric Matrix Protein; Child; Child, Preschool; Collagen Type II; Connective Tissue Diseases; Dwarfism; Female; Gene Expression; Genetic Testing; Hearing Loss, Sensorineural; High-Throughput Nucleotide Sequencing; Homeodomain Proteins; Humans; Male; Mutation; Noonan Syndrome; Osteochondrodysplasias; Protein Tyrosine Phosphatase, Non-Receptor Type 11; Retinal Detachment; SOS1 Protein; Transcription Factors | 2018 |