dapi has been researched along with Deficiency, Mental in 4 studies
DAPI: RN given refers to parent cpd.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 3 (75.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Leclercq, S | 1 |
| Maincent, K | 1 |
| Baverel, F | 1 |
| Tessier, DL | 1 |
| Letourneur, F | 1 |
| Lebbar, A | 1 |
| Dupont, JM | 1 |
| Garavelli, L | 1 |
| Zollino, M | 1 |
| Mainardi, PC | 1 |
| Gurrieri, F | 1 |
| Rivieri, F | 1 |
| Soli, F | 1 |
| Verri, R | 1 |
| Albertini, E | 1 |
| Favaron, E | 1 |
| Zignani, M | 1 |
| Orteschi, D | 1 |
| Bianchi, P | 1 |
| Faravelli, F | 1 |
| Forzano, F | 1 |
| Seri, M | 1 |
| Wischmeijer, A | 1 |
| Turchetti, D | 1 |
| Pompilii, E | 1 |
| Gnoli, M | 1 |
| Cocchi, G | 1 |
| Mazzanti, L | 1 |
| Bergamaschi, R | 1 |
| De Brasi, D | 1 |
| Sperandeo, MP | 1 |
| Mari, F | 1 |
| Uliana, V | 1 |
| Mostardini, R | 1 |
| Cecconi, M | 1 |
| Grasso, M | 1 |
| Sassi, S | 1 |
| Sebastio, G | 1 |
| Renieri, A | 1 |
| Silengo, M | 1 |
| Bernasconi, S | 1 |
| Wakamatsu, N | 1 |
| Neri, G | 1 |
| Jacoby, M | 1 |
| Cox, JJ | 1 |
| Gayral, S | 1 |
| Hampshire, DJ | 1 |
| Ayub, M | 1 |
| Blockmans, M | 1 |
| Pernot, E | 1 |
| Kisseleva, MV | 1 |
| Compère, P | 1 |
| Schiffmann, SN | 1 |
| Gergely, F | 1 |
| Riley, JH | 1 |
| Pérez-Morga, D | 1 |
| Woods, CG | 1 |
| Schurmans, S | 1 |
| Lin, MS | 1 |
| Huynh, KH | 1 |
| Fujimoto, A | 1 |
| Wilson, MG | 1 |
1 review available for dapi and Deficiency, Mental
| Article | Year |
|---|---|
Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literature.
Topics: Abnormalities, Multiple; Adolescent; Aging; Child; Child, Preschool; Chromosomes, Artificial, Bacter | 2009 |
3 other studies available for dapi and Deficiency, Mental
| Article | Year |
|---|---|
Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U-type exchange model.
Topics: Chromosome Aberrations; Chromosome Breakage; Chromosome Disorders; Chromosome Inversion; Chromosomes | 2009 |
INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse.
Topics: Animals; Bardet-Biedl Syndrome; Cell Line; Cell Nucleus; Cells, Cultured; Chromones; Cilia; Culture | 2009 |
Lack of specificity of DA/DAPI fluorescence.
Topics: Adult; Chromosome Aberrations; Chromosome Banding; Chromosomes, Human, Pair 10; Chromosomes, Human, | 1990 |