基因突变分析是开展遗传咨询和产前诊断的重要工具。
Gene mutation analysis is the important tool for genetic counseling and prenatal diagnosis.
建议将此突变位点检测运用于遗传咨询、产前诊断、新生儿和不明原因感音神经性聋患者的基因筛查中。
It is suggested to utilize this detection for genetic counseling, prenatal diagnosis, and the genetic screening of neonates and the sensorineural hearing loss with unknown reason.
随着分子遗传学技术在致聋基因的克隆、鉴定等方面应用的进展，使得为某些家庭进行遗传咨询成为可能。
Recent advances within molecular genetics to identify the genes for deafness mean that it is now possible for genetic counseling services to offer genetic testing for deafness to certain families.
目的探索一种更简便和更特异的方法，用于血友病a的基因诊断及其家系遗传咨询。
Objective To find out a simple and specific method for genetic diagnosis of hemophilia a and identification of carriers.
的基因型诊断，不仅可进行遗传咨询，而且有可能指导临床治疗。
So far, a clear genetic disease genes have a lot of epilepsy, epilepsy diagnosis genotypes, not only for genetic counseling, and may guide clinical treatment.
的基因型诊断，不仅可进行遗传咨询，而且有可能指导临床治疗。
So far, a clear genetic disease genes have a lot of epilepsy, epilepsy diagnosis genotypes, not only for genetic counseling, and may guide clinical treatment.
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