nsc-172755 has been researched along with Chromosome Deletion in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Abramovicz, M; Alao, MJ; Arveiler, B; Hans, Ch; Lacombe, D; Lalèyè, A; Lalya, F; Morice-Picard, F; Rooryck, C | 1 |
| Chan, L; Powars, DR; Schroeder, WA | 1 |
1 review(s) available for nsc-172755 and Chromosome Deletion
| Article | Year |
|---|---|
Beta S-gene-cluster haplotypes in sickle cell anemia: clinical implications.
Topics: Anemia, Sickle Cell; Benin; Central African Republic; Chromosome Deletion; Chromosomes, Human, Pair 11; Fetal Hemoglobin; Globins; Haplotypes; Hemoglobin, Sickle; Humans; Life Tables; Polymorphism, Restriction Fragment Length; Prognosis; Risk Factors; Senegal; Severity of Illness Index; Survival Rate; Thalassemia; United States | 1990 |
1 other study(ies) available for nsc-172755 and Chromosome Deletion
| Article | Year |
|---|---|
Blepharophimosis, ptosis, epicanthus inversus syndrome with translocation and deletion at chromosome 3q23 in a black African female.
Topics: Benin; Black People; Blepharophimosis; Chromosome Deletion; Chromosomes, Human, Pair 3; Female; Forkhead Box Protein L2; Forkhead Transcription Factors; Humans; Infant; Menopause, Premature; Skin Abnormalities; Translocation, Genetic | 2012 |