Page last updated: 2024-08-26

dihydrorhodamine 123 and Autosomal Chromosome Disorders

dihydrorhodamine 123 has been researched along with Autosomal Chromosome Disorders in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chan, KW; Chang, YH; Chiang, BL; Lau, YL; Yu, HH1

Other Studies

1 other study(ies) available for dihydrorhodamine 123 and Autosomal Chromosome Disorders

ArticleYear
A new autosomal recessive, heterozygous pair of mutations of CYBA in a patient with chronic granulomatous disease.
    Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology, 2010, Volume: 105, Issue:2

    Topics: Child; Chromosome Disorders; Chromosomes, Human, Pair 16; DNA Mutational Analysis; Female; Genes, Recessive; Granulomatous Disease, Chronic; Heterozygote; Humans; Mutation; NADPH Oxidases; Pedigree; Reproducibility of Results; Rhodamines; Sensitivity and Specificity

2010