[HTML][HTML] 非综合征型聋家系SLC26A4基因复合杂合突变
贾薇， 索利敏， 范林静， 董佩， 张磊… - 中国耳鼻咽喉颅 …, 2024 - zgebyheldwkzz.ijournals.cn
… The possible pathogenic genes and mutation sites of this patient were identified, and the
relevant mutation sites of the parents were further verified by Sanger sequencing method. The …
relevant mutation sites of the parents were further verified by Sanger sequencing method. The …
海南省新生儿耳聋基因携带情况分析.
范霞林， 樊利春， 黄垂灿， 吴维佳… - China Tropical …, 2022 - search.ebscohost.com
… Results A total of 7 124 newborns were included in the study through informed consent, 219
cases of deafness gene mutation were detected with the detection rate of deafness gene of …
cases of deafness gene mutation were detected with the detection rate of deafness gene of …