adenine has been researched along with Kallmann Syndrome in 1 studies
Kallmann Syndrome: A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait.
| 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 |
|---|---|
| Bailleul-Forestier, I | 1 |
| Gros, C | 1 |
| Zenaty, D | 1 |
| Bennaceur, S | 1 |
| Leger, J | 1 |
| de Roux, N | 1 |
1 other study available for adenine and Kallmann Syndrome
| Article | Year |
|---|---|
Dental agenesis in Kallmann syndrome individuals with FGFR1 mutations.
Topics: Adenine; Adolescent; Adult; Anodontia; Arginine; Bicuspid; Child, Preschool; Cleft Palate; Cysteine; | 2010 |