arginine vasopressin has been researched along with Craniofacial Abnormalities 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 |
|---|---|
| Alatzoglou, KS; Dattani, MT; Farooqi, IS; Gaston-Massuet, C; Gerrelli, D; Gregory, LC; Kavanaugh, SI; Martinez-Barbera, JP; McCabe, MJ; Pitteloud, N; Puelles, E; Raza, J; Signore, M; Tsai, PS; Tziaferi, V; Walker, J | 1 |
1 other study(ies) available for arginine vasopressin and Craniofacial Abnormalities
| Article | Year |
|---|---|
Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction.
Topics: Agenesis of Corpus Callosum; Arginine Vasopressin; Craniofacial Abnormalities; DNA Mutational Analysis; Female; Fibroblast Growth Factor 8; Holoprosencephaly; Human Growth Hormone; Humans; Hydrocortisone; Hypothalamic Diseases; Hypothalamo-Hypophyseal System; Immunohistochemistry; In Situ Hybridization; Infant; Magnetic Resonance Imaging; Mutation; Pituitary Diseases; Pituitary Gland; Prosencephalon; Receptor, Fibroblast Growth Factor, Type 1; Septo-Optic Dysplasia; Thyrotropin | 2011 |