are most frequently used: resctriction
enzyme analysis, the heteroduplex
analysis, ARMS, reverse hybridization
and OLA.
Cystic fibrosis:囊胞性纤维症
heteroduplex:异源双链核酸分子
simultaneously:同时地;
deletion:缺失
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4. Phenylketonuria is an inborn error of metabolism resulting from a deficiency of phenylalanine hydroxylase. There are many techniques that can be used to mutation screening, such as PCR-STR, PCR-SSCP, PCR-RFLP, PCR-DGCE, and so on.
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评估基因的存在和缺 陷通常以DNA为材料
评估基因的表达量则 以基因转录或翻译 RNA/蛋白质为对象
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Section 1 遗传性疾病分子诊断的策略
4p16.3. HD can be accurately confirmed or excluded by PCR-based assay. Huntington’s disease(HD) :亨廷顿病