west china medical publishers

west china medical publishers

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find Keyword "遗传性/诊断" 2 results

孤发性Leber遗传性视神经病Wallace突变的检测

Chinese Journal of Ocular Fundus Diseases 2000, 16(2): 79-80

Release date：2016-09-02 06:05 Export PDF Favorites Scan
Primary mutation detection of mitochondrial DNA(mtDNA)in Leber′s hereditary optic neuropathy patients

Chinese Journal of Ocular Fundus Diseases 1999, 15(4): 223-226

Optic atrophy,hereditary／diagnosis; Polymerase chain reaction; DNA,mitochondrial; Point　mutation; Sequence analysis

Release date：2016-09-02 06:07 Export PDF Favorites Scan