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METHOD OF PRENATAL MOLECULAR DIAGNOSIS OF DOWN SYNDROME AND OTHER TRISOMIC DISORDERS
METHOD OF PRENATAL MOLECULAR DIAGNOSIS OF DOWN SYNDROME AND OTHER TRISOMIC DISORDERS
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机译:唐氏综合症及其他创伤性疾病的产前分子诊断方法
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摘要
The present invention encompasses a method of diagnosing chromosomal trisomy in a human subject. In one embodiment, the method comprises pyrosequencing at least one single nucleotide polymorphism on a chromosome being assessed for trisomy, where the SNP comprises two alleles.
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