ammonium hydroxide has been researched along with Abnormalities, Autosome in 10 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) |
| "Individual indicators of chromosomal aberrations varied by 2-3 times irrespective of the length of service." | 1.28 | [Assessment of the effects of a set of factors in the production of nitrogen fertilizers on chromosomes in peripheral blood lymphocytes of female workers and health status of their newborn infants]. ( Sazonova, LA; Sidenko, AT; Vazhnik, LA, 1989) |
| "A male infant with a partial trisomy 18 and a 46,XY, --21, t(18;21)(18qter replaced by 18q12::21 p13 replaced by 21 qter) chromosome complement is described." | 1.26 | Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18. ( Barg, GA; Denton, TE; Gardner, LI; Howell, WM; Neu, RL; Ortega, CC; Pinto, W, 1976) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (70.00) | 18.7374 |
| 1990's | 1 (10.00) | 18.2507 |
| 2000's | 1 (10.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (10.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ifuku, T | 1 |
| Suzuki, S | 1 |
| Nagatomo, Y | 1 |
| Yokoyama, R | 1 |
| Yamamura, Y | 1 |
| Nakatani, K | 1 |
| Qureshi, IA | 1 |
| Rao, KV | 1 |
| Sabina, RL | 1 |
| Neu, RL | 1 |
| Ortega, CC | 1 |
| Barg, GA | 1 |
| Pinto, W | 1 |
| Gardner, LI | 1 |
| Howell, WM | 1 |
| Denton, TE | 1 |
| Sidenko, AT | 1 |
| Sazonova, LA | 1 |
| Vazhnik, LA | 1 |
| Watanabe, S | 1 |
| Hilschmann, N | 1 |
| Tancredi, F | 1 |
| Striano, S | 1 |
| Ragonese, G | 1 |
| Cedrola, G | 1 |
| Guazzi, GC | 1 |
| Colombo, JP | 1 |
| Matsuda, I | 1 |
| Sugai, M | 1 |
| Kajii, T | 1 |
| Györy, AZ | 1 |
| Edwards, KD | 1 |
3 reviews available for ammonium hydroxide and Abnormalities, Autosome
| Article | Year |
|---|---|
Sparse-fur (spf) mouse as a model of hyperammonemia: alterations in the neurotransmitter systems.
Topics: Ammonia; Animals; Chromosome Aberrations; Chromosome Disorders; Disease Models, Animal; Gene Express | 1997 |
Myoadenylate deaminase deficiency. A common inherited defect with heterogeneous clinical presentation.
Topics: Alleles; Ammonia; AMP Deaminase; Chromosome Aberrations; Chromosome Disorders; Exercise Test; Genes, | 2000 |
Congenital disorders of the urea cycle and ammonia detoxication.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Animals; Brain; Chromosome Aberrations; Fetus; Humans | 1971 |
7 other studies available for ammonium hydroxide and Abnormalities, Autosome
| 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 |
Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18.
Topics: Ammonia; Chromosome Aberrations; Chromosomes, Human, 16-18; Chromosomes, Human, 21-22 and Y; Humans; | 1976 |
[Assessment of the effects of a set of factors in the production of nitrogen fertilizers on chromosomes in peripheral blood lymphocytes of female workers and health status of their newborn infants].
Topics: Adult; Air Pollutants, Occupational; Ammonia; Carbon Monoxide; Chemical Industry; Chromosome Aberrat | 1989 |
[The primary structure of a monoclonal kappa-type immunoglobulin L-chain of subgroup I (Bence-Jones Protein Hau): subdivision within subgroups].
Topics: Amino Acid Sequence; Amino Acids; Ammonia; Binding Sites; Chemical Precipitation; Chromosome Aberrat | 1970 |
[Argininosuccinic aciduria with and without hyperammoniemia. Study of 2 cases].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Child; Child Behavior Disorders; Child, | 1973 |
Ornithine loading test in Lowe's syndrome.
Topics: Abnormalities, Multiple; Amino Acids; Ammonia; Chromosome Aberrations; Chromosome Disorders; Eye Dis | 1970 |
Renal tubular acidosis. A family with an autosomal dominant genetic defect in renal hydrogen ion transport, with proximal tubular and collecting duct dysfunction and increased metabolism of citrate and ammonia.
Topics: Acidosis, Renal Tubular; Adult; Aged; Ammonia; Chromosome Aberrations; Chromosome Disorders; Citrate | 1968 |