Page last updated: 2024-08-26

nsc-172755 and Thalassemias

nsc-172755 has been researched along with Thalassemias in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19902 (66.67)18.7374
1990's1 (33.33)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Baya, H; Dunda-Belkhodja, O; Jaeger, G; Labie, D; Nagel, RL; Pagnier, J; Teyssier, J; Zohoun, I1
Chan, L; Powars, DR; Schroeder, WA1
Baudin, V; Fabry, ME; Labie, D; Nagel, RL; Pagnier, J; Wajcman, H; Zohoun, I1

Reviews

1 review(s) available for nsc-172755 and Thalassemias

ArticleYear
Beta S-gene-cluster haplotypes in sickle cell anemia: clinical implications.
    The American journal of pediatric hematology/oncology, 1990,Fall, Volume: 12, Issue:3

    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

Other Studies

2 other study(ies) available for nsc-172755 and Thalassemias

ArticleYear
alpha-Thalassemia among sickle cell anemia patients in various African populations.
    Human genetics, 1984, Volume: 68, Issue:4

    Topics: Adolescent; Adult; Anemia, Sickle Cell; Benin; Central African Republic; Child; Child, Preschool; Epistasis, Genetic; Gene Frequency; Humans; Infant; Senegal; Thalassemia

1984
Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type.
    The New England journal of medicine, 1985, Apr-04, Volume: 312, Issue:14

    Topics: Adult; Analysis of Variance; Anemia, Sickle Cell; Benin; Child; Child, Preschool; Erythrocyte Count; Fetal Hemoglobin; Globins; Haploidy; Hematocrit; Humans; Senegal; Thalassemia

1985