Fluorescence in situ hybridization of multicolor fibers
Source : Molecular Cytogenetics Techniques and Applications
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Experiments to describe chromosomal structural abnormalities by comparative genomic hybridization
Comparative Genomic Hybridization (CGH) is a molecular cytogenetic technique capable of characterizing, in a one-step genome-wide screening procedure, additions
Diagnosis of Fanconi anemia (congenital myelodysplasia)--dioxobutane (dibutyl epoxide) detection assay
Fanconi anemia (FA) is an autosomal recessive syndrome characterized by progressive bone marrow failure and an increased risk of malignancies, particularly acut
Experimental application of fluorescence in situ hybridization in the preimplantation diagnosis of aneuploidy
Pre-implantation Genetic Diagnosis (PGD), as a major new method of preventing genetic disorders, avoids the need for prenatal diagnosis and the possibility of t
Experiments on the effect of environment on gene expression in Drosophila
Many aspects of phenotype are influenced by the genetic composition of an organism and the environment in which it lives, so it can be said that phenotype is a
Experimental molecular detection of uniparental diploids
Uniparental diploid (UPD) cells can have a normal cytogenetic karyotype but an imbalance in parental contributions. The diagnosis of uniparental diploidy involv
Meiosis mapping experiment
Currently, genetic mapping techniques can be used as a way to monitor the means of genomic manipulation, which needs to be realized through the use of molecular
Fluorescent genotyping screening for tiny subtelomeric rearrangement assay
Our results strongly support the notion that microtelomeric rearrangements play a very important role in spontaneous mental retardation (approximately 12% in ou
Nuclease digestion of purified genomic DNA by Micrococcus spp.
MNase can cut DNA non-randomly. therefore, to determine how this naturally non-random pattern is affected by nuclear proteins such as histones, it is important