ammonium hydroxide has been researched along with 22q11.2 Deletion Syndrome in 1 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Several genetic chromosomal abnormalities, including 22qDS, and CPSS have similar symptoms, and neurodevelopmental abnormalities, particularly those caused by PSE, may be difficult to diagnose." | 1.72 | Congenital portosystemic venous shunt associated with 22q11.2 deletion syndrome: a case report. ( Ifuku, T; Nagatomo, Y; Nakatani, K; Suzuki, S; Yamamura, Y; Yokoyama, R, 2022) |
| 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 | 0 (0.00) | 24.3611 |
| 2020's | 1 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ifuku, T | 1 |
| Suzuki, S | 1 |
| Nagatomo, Y | 1 |
| Yokoyama, R | 1 |
| Yamamura, Y | 1 |
| Nakatani, K | 1 |
1 other study available for ammonium hydroxide and 22q11.2 Deletion Syndrome
| Article | Year |
|---|---|
Congenital portosystemic venous shunt associated with 22q11.2 deletion syndrome: a case report.
Topics: Ammonia; Bile Acids and Salts; Child, Preschool; Chromosome Aberrations; DiGeorge Syndrome; Humans; | 2022 |