Compounds > diepoxybutane
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diepoxybutane and Chromosomal Fragility

diepoxybutane has been researched along with Chromosomal Fragility in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's1 (25.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ghosh, K; Korgaonkar, S; Vundinti, BR1
Badell, I; Beléndez, C; Bueren, JA; Callén, E; Casado, JA; Castella, M; Cela, E; Dasí, Á; de Heredia, CD; de Toledo, JS; Estella, J; Ferro, T; Figuera, Á; Gómez, P; Madero, L; Molinés, A; Muñoz, A; Olivé, T; Pujol, R; Ramírez, MJ; Rodríguez-Villa, A; Sevilla, J; Surrallés, J; Talavera, M; Tapia, M1
Gibson, R; Hajianpour, A; Khallouf, KA; Mathew, CG; Milner, RD1
Burke, LW; Grant, SG; Latimer, JJ; Thull, D; Wenger, SL1

Other Studies

4 other study(ies) available for diepoxybutane and Chromosomal Fragility

ArticleYear
Clinical, genetic and cytogenetic study of Fanconi anemia in an Indian population.
    Hematology (Amsterdam, Netherlands), 2010, Volume: 15, Issue:1

    Topics: Adolescent; Carcinoma, Squamous Cell; Cells, Cultured; Child; Child, Preschool; Chromosome Breakage; Chromosome Fragility; Chromosomes, Human; Consanguinity; Epoxy Compounds; Fanconi Anemia; Female; Humans; India; Infant; Leukemia, Myeloid; Male; Mitomycin; Myelodysplastic Syndromes; Young Adult

2010
Chromosome fragility in patients with Fanconi anaemia: diagnostic implications and clinical impact.
    Journal of medical genetics, 2011, Volume: 48, Issue:4

    Topics: Chromosome Fragility; Cross-Linking Reagents; Epoxy Compounds; Fanconi Anemia; Humans; Mitomycin; Mosaicism; Phenotype

2011
A new autosomal recessive anomaly mimicking Fanconi's anaemia phenotype.
    Archives of disease in childhood, 1993, Volume: 68, Issue:1

    Topics: Abnormalities, Multiple; Child; Child, Preschool; Chromosome Fragility; Chromosome Mapping; Epoxy Compounds; Fanconi Anemia; Female; Genes, Recessive; Growth Disorders; Humans; Infant; Male; Pedigree; Syndrome

1993
Analysis of genomic instability using multiple assays in a patient with Rothmund-Thomson syndrome.
    Clinical genetics, 2000, Volume: 58, Issue:3

    Topics: Adult; Blood Group Antigens; Child; Child, Preschool; Chromosome Fragility; DNA Damage; DNA Repair; Epoxy Compounds; Erythrocytes; Female; Flow Cytometry; Glycophorins; Humans; Infant; Infant, Newborn; Karyotyping; Loss of Heterozygosity; Lymphocytes; Male; Mitomycin; Mutation; Rothmund-Thomson Syndrome

2000