ObjectiveIn Caucasian population, the most common molecular basis for C8β deficiency is a single C→T transition in exon 9 of C8β gene resulting in a stop codon.

Study on p16 gene deletion and promoter 5 CpG island hypomethylation in coal-burning arsenism patients;

Gene clone and deletion of ApxIICA of Actinobacillus pleuropneumoniaeserotype 7 strain 25-4;

Detection of p16 gene deletion and methylation in esophageal squamous cell carcinoma tissue;

Detection of muscular dystrophy gene deletions by 9 pairs of primers;

Investigation on p16 gene deletion in tissues of primary squamous cell carcinoma of esophagus;