rubidium has been researched along with Facies 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 |
|---|---|
| Arntzen, KA; Bakkers, J; Dybesland, AR; Emfinger, CH; Gunn, J; Hansen, GÅM; Harter, T; Hjellnes, H; Huang, Y; Kamel, SM; Kovacs, A; Massink, M; McClenaghan, C; Müller, KI; Nichols, CG; Remedi, MS; Roessler, HI; Sala-Rabanal, M; Savelberg, S; Singareddy, SS; Smeland, MF; Tessadori, F; Van Ghelue, M; van Haaften, G; Wozniak, DF | 1 |
1 other study(ies) available for rubidium and Facies
| Article | Year |
|---|---|
ABCC9-related Intellectual disability Myopathy Syndrome is a K
Topics: Adenosine Triphosphate; Adolescent; Adult; Amino Acid Sequence; Animals; Cardiomegaly; Cell Line; Channelopathies; Child; Disease Models, Animal; Facies; Female; Genetic Diseases, X-Linked; Genetic Predisposition to Disease; Heart; Heart Diseases; Homozygote; Humans; Hypertrichosis; Intellectual Disability; Male; Mediator Complex; Membrane Proteins; Mice; Muscular Diseases; Mutation; Neurodevelopmental Disorders; Osteochondrodysplasias; Pedigree; Phenotype; Rubidium; Sulfonylurea Receptors; Whole Genome Sequencing; Young Adult; Zebrafish | 2019 |