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Southeast Asian J Trop Med Public Health ; 1995 ; 26 Suppl 1(): 92-5
Article in English | IMSEAR | ID: sea-31797

ABSTRACT

The chromosome in situ suppression hybridization or chromosome painting technic was applied to confirm and eliminate the markers involving chromosome 21 segments using a chromosome 21 DNA library. The library ATCCLL21SNO2 was amplified, directly biotinylated using the polymerase chain reaction. The results demonstrated a translocation of chromosome 21 material on chromosome 2 and X and eliminate the origin of the marker. Thus, the technique provides an important tool to complement the conventional G-banding technic.


Subject(s)
Abnormalities, Multiple/genetics , Adult , Chromosomes, Human, Pair 2 , Chromosomes, Human, Pair 21 , Down Syndrome/diagnosis , Female , Gene Library , Genetic Markers , Genetic Carrier Screening , Humans , Infant, Newborn , Intellectual Disability/genetics , Metaphase , Translocation, Genetic , X Chromosome
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