Method 32 families with HNPCC were registered and followed up.
方法对随访登记的32家系进行随访和回顾。
So it is necessary to set up criteria for diagnosis of HNPCC in Chinese.
建立中国人的HNPCC诊断标准是必要的。
Blood tests are now available to test for FAP, AFAP, MYH, and HNPCC hereditary colon cancer syndromes.
血液化验，现已是测定fap,AFAP,MY H，与HNPCC等遗传性大肠癌综合征的方法。
It is necessary to detect the large intragenic MMR genes deletions in the molecular detection of HNPCC.
在分子遗传学检测中有必要开展MMR基因大片段缺失的检测。
Methods Six HNPCC kindreds were investigated, including the patient's gender, age of diagnosis, sites of cancer, etc.
方法对我院6个HNPCC家系进行调查，记录患者性别、发病年龄、肿瘤部位等。
Objective To investigate the clinicopathological and molecular genetic characteristics of Chinese hereditary nonpolyposis colorectal cancer (HNPCC) pedigrees.
目的了解国人遗传性非息肉病性结直肠癌（HNPCC）的临床病理及分子遗传学特征。
Objective: to characterize the clinical features of Chinese HNPCC families and to screen the mutations of a poly (a) 8 tract in M3 cholinergic receptor gene in these families.
目的：分析中国人遗传性非息肉病性大肠癌(HNPCC)家系的临床特征并检测这些家系中M3胆碱能受体基因(A)8区的突变情况。
Objective: to characterize the clinical features of Chinese HNPCC families and to screen the mutations of a poly (a) 8 tract in M3 cholinergic receptor gene in these families.
目的：分析中国人遗传性非息肉病性大肠癌(HNPCC)家系的临床特征并检测这些家系中M3胆碱能受体基因(A)8区的突变情况。
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