Keyword [Splicing mutation] Result: 21 - 27 | Page: 2 of 2 21.  Detection And Functional Study Of Pathogenic Mutations That Associated With Congenital Cataract 22.  Clinical Analysis And Gene Mutation Of Type 1 Neurofibroma With Skull Defect 23.  Mutation Detection And Functional Research About Hereditary Aortic Diseases Based On Next-Generation Sequencing 24.  Study The Novel Splicing Mutation In Wiskott-Aldrich Syndrome And Its Pathogenic Mechanism 25.  Identification And Characterization Of Novel Hereditary Multiple Exostoses-associated Mutations 26.  The Role And Mechanism Of AIFM1 In Auditory Neuropathy And Presbycusis 27.  Identification And Analysis Of Copy Number Variation And Splicing Mutation Of FBN1 Gene In Marfan Syndrome   <<First  <Prev  Next>  Last>>  Jump to

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