trolamine salicylate has been researched along with Absence of Corpus Callosum 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 |
---|---|
Claes, C; Collins, F; Flaherty, M; Pinner, J; Schrauwen, I; Sommen, M; Van Camp, G | 1 |
1 other study(ies) available for trolamine salicylate and Absence of Corpus Callosum
Article | Year |
---|---|
Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome.
Topics: Agenesis of Corpus Callosum; Arthritis; Base Sequence; Collagen Diseases; Connective Tissue Diseases; Eye; Hearing Loss, Sensorineural; Hernias, Diaphragmatic, Congenital; Humans; Low Density Lipoprotein Receptor-Related Protein-2; Magnetic Resonance Imaging; Molecular Sequence Data; Mutation, Missense; Myopia; Pedigree; Phenotype; Proteinuria; Renal Tubular Transport, Inborn Errors; Retinal Detachment; Sequence Analysis, DNA | 2014 |