目的调查DXYS267基因座遗传多态性，研究该座位伴性遗传单核苷酸的特征及其法医学应用价值。
Objective To investigate the polymorphism of DXYS267 locus in China Han population and find the application and characters of its Y-specific single nucleotide substitutions.
目的探讨遗传性痉挛性截瘫伴薄型胼胝体(HSPTCC)的临床特征。
Objective To explore the clinical characteristics of hereditary spastic paraplegia with thin corpus callosum (HSP TCC).
目的分析伴前庭水管扩大(eva)的遗传性耳聋患者SLC26 A 4基因的突变特点，探讨该病行人工耳蜗植入时应注意的问题。
Objective to probe the problems that should be paid attention to in cochlea implantation for inherited deafness patients with EVA and to detect the SLC26A4 gene mutation underlying the disease.
目的从分子遗传水平进行基因多态性研究，以探讨2型糖尿病易伴发冠心病的内在原因。
Objective To explore the association of type 2 diabetes with coronary heart disease (CHD), from gene polymorphism analysis.
目的：探讨单胺氧化酶a和单胺氧化酶b基因与伴精神病性症状双相情感性障碍间的遗传关联性。
Objective: to investigate the genetic association between MAOA and MAOB genes and the bipolar affective disorder with psychiatric symptoms.
目的：探讨单胺氧化酶a和单胺氧化酶b基因与伴精神病性症状双相情感性障碍间的遗传关联性。
Objective: to investigate the genetic association between MAOA and MAOB genes and the bipolar affective disorder with psychiatric symptoms.
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