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Keyword [pathogenic mutation]
Result: 21 - 23 | Page: 2 of 2
21.
Clinical Phenotype And Identification Of The Causative Genes For Three Families With Hearing Loss And Correlation Analysis On NsSNPs Of WFS1 Gene And Diseases
22.
Identification Of New Pathogenic Mutation For Alport Syndrome And Establishment Of Patient-derived Induced Pluripotent Stem Cells
23.
Study On The Function Of A Case Of Werner Syndrome Caused By Novel Pathogenic Mutation Of WRN Gene
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