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Diagnostic kit for prenatal detection of trisomy 13, comprises primer pairs specific for amplification of short tandem repeat regions in chromosome 13
Diagnostic kit for prenatal detection of trisomy 13, comprises primer pairs specific for amplification of short tandem repeat regions in chromosome 13
Diagnostic kit for detecting trisomy 13 in a human fetus comprises at least two pairs of oligonucleotide primers suitable for amplification, by polymerase chain reaction (PCR), of both strands of a target DNA sequence, i.e. a short tandem repeat region (X) of human chromosome 13. Independent claims are also included for the following: (1) microarray for detecting trisomy 13, especially a DNA chip, comprising an array of many separate fields, at least one of which carries an oligonucleotide able to hybridize to DNA that is part of X; and (2) method for detecting trisomy 13.
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