1991
DOI: 10.1016/0165-4608(91)90195-z
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Translocation (8;21) in acute nonlymphocytic leukemia delineated by chromosomal in situ suppression hybridization

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Cited by 9 publications
(3 citation statements)
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“…Recent studies demonstrated that the newly developed FISH method has provided additional resources to improve the analysis of chromosome abnormalities. It can verify the involved segments of the chromosomes not only in metaphase but also in interphase cells, and help interpret marker chromosomes that cannot be identified by banding techniques along [10][11][12][13][14][15]. However, the FISH method itself has some restrictions: first, its performance needs freshly made metaphase spreads; second, FISH results from unbanded slides must be interpreted conservatively regarding complex karyotypes.…”
Section: Discussionmentioning
confidence: 99%
“…Recent studies demonstrated that the newly developed FISH method has provided additional resources to improve the analysis of chromosome abnormalities. It can verify the involved segments of the chromosomes not only in metaphase but also in interphase cells, and help interpret marker chromosomes that cannot be identified by banding techniques along [10][11][12][13][14][15]. However, the FISH method itself has some restrictions: first, its performance needs freshly made metaphase spreads; second, FISH results from unbanded slides must be interpreted conservatively regarding complex karyotypes.…”
Section: Discussionmentioning
confidence: 99%
“…It is very often extremely difficult to assign small pieces of rearranged chromosomal material by banding techniques, whereas painting of the chromosome in question visualizes even small translocated material of the targeted chromosome [156]. Chromosome painting can be used for detecting numerical as well as structural aberrations of a particular chromosome (e.g., chromosome 21 aberrations diagnostic for Down's Syndrome) [48,59,67,69,157].…”
Section: Clinical Applicationsmentioning
confidence: 99%
“…It has also been widely used for molecular cytotaxonomy, for example of primates (Muller et al 1999; Wienberg et al 1990), mutagenicity testing (Marshall and Obe 1998) and radiation biology (Gray et al 1992). High resolution CP-based analyses have become especially important to pre-, neo- and postnatal clinical diagnostics of various chromosomal aberrations associated with human diseases and malignancies (Gray and Pinkel 1992; Popp et al 1991; Tkachuk et al 1991; Weise et al 2003; Xu et al 2010). …”
Section: Introductionmentioning
confidence: 99%