Results The SSCP analysis showed false positive results.
结果：SSCP分析存在假阳性结果。
This result showed that PCR-SSCP analysis could be effectively used for the direct gene diagnosis of phenylketonuria.
SSCP分析法可有效地用于苯丙酮尿症的基因诊断。
Conclusions Appropriate LPA concentration, running temperature and running voltage can improve ce performance in SSCP analysis.
结论：调整适宜的LPA浓度、分离温度和分离电压可提高CE分析SSCP的效率。
By PCR-SSCP analysis, 17 PCR products were identified with different mobility of single strand DNA in propositus. 9 suspectable mutations were revealed with DNA sequencing analysis.
SSCP分析发现17个外显子pcr产物单链dna迁移率异常，通过DNA直接测序发现9个外显子可疑突变，但反向测序均未能证实。
Methods: The hypermethylation was examined by methyl sensitive restrictive DNA endoenzyme analysis in 34 cases of angioreticuloma and the VHL gene mutations detected by PCR SSCP analysis.
方法：采用PCRSSCP法检测血管网织细胞瘤中VHL基因的突变率及甲基化，敏感限制性内切酶消化法检测血管网织细胞瘤中VHL基因的异常甲基化率。
Single strand conformation polymorphism (SSCP) essay and sequence analysis of the PCR product were used to ascertain the gene mutation.
方法应用PCR及单链构象多态性(SSCP)分析技术结合基因序列测定方法确定突变类型。
Methods immunohistochemistry in 52 cases of nasopharyngeal carcinoma PTEN gene expression, the use of PCR SSCP silver staining, DNA sequencing analysis to detect PTEN gene mutation in exon 5, 8.
方法采用免疫组化检测52例鼻咽癌中pten基因的表达，利用PCRSSCP银染、DNA测序分析等方法检测pten基因第5、8外显子突变。
PCR and single strand conformation polymorphism analysis (SSCP) were combined with DNA sequencing confirmation to screen all 28 exons of SCN5A gene.
采用PCR单链构象多态性技术（SSCP）结合DNA序列测定证实，对病人SCN5A的全部2 8个外显子进行突变检测。
PCR and single strand conformation polymorphism analysis (SSCP) were combined with DNA sequencing confirmation to screen all 28 exons of SCN5A gene.
采用PCR单链构象多态性技术（SSCP）结合DNA序列测定证实，对病人SCN5A的全部2 8个外显子进行突变检测。
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