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논문 유사도에 따라 DBpia 가 추천하는 논문입니다. 함께 보면 좋을 연관 논문을 확인해보세요!
Brain Somatic Mutations in Epileptic Disorders
Molecules and Cells
2018 .10
Comparative analysis of cancer gene mutations using targeted sequencing in matched primary and recurrent gastric cancers after chemotherapy
Genes & Genomics
2022 .11
Effect of Next-Generation Exome Sequencing Depth for Discovery of Diagnostic Variants
Genomics & informatics
2015 .01
Identification of novel alleles induced by EMS-mutagenesis in key genes of kernel hardness and starch biosynthesis in wheat by TILLING
Genes & Genomics
2017 .01
Mutation Hotspots in the β-catenin Gene : Lessons from Human Cancer Genome Databases
Molecules and Cells
2019 .01
Whole exome sequencing revealed novel variants in consanguineous Pakistani families with intellectual disability
Genes & Genomics
2021 .01
Genotype–phenotype correlation of Charcot-Marie-Tooth type 1E patients with PMP22 mutations
Genes & Genomics
2016 .01
Comparison of the Genetic Alterations between Primary Colorectal Cancers and Their Corresponding Patient-Derived Xenograft Tissues
Genomics & informatics
2018 .01
A novel homozygous mutation in SZT2 gene in Saudi family with developmental delay, macrocephaly and epilepsy
Genes & Genomics
2018 .01
Four mutations identified in Chinese families with autosomal dominant congenital cataracts by next-generation sequencing
Genes & Genomics
2024 .08
Whole-exome sequencing identifies a novel LRAT mutation underlying retinitis punctata albescens in a consanguineous Pakistani family
Genes & Genomics
2015 .01
Identification and Clinical Implications of Novel MYO15A Mutations in a Non-consanguineous Korean Family by Targeted Exome Sequencing
Molecules and Cells
2015 .09
Molecular insights into TP53 mutation (p. Arg267Trp) and its connection to Choroid Plexus Carcinomas and Li-Fraumeni Syndrome
Genes & Genomics
2024 .08
Whole-exome sequencing identifies two novel missense mutations (p.L111P and p.R3048C) of RYR3 in a Vietnamese patient with autism spectrum disorders
Genes & Genomics
2017 .01
Four novel mutations in the androgen receptor gene from Vietnamese patients with androgen insensitivity syndrome
Genes & Genomics
2023 .04
Mutational Analysis of Extranodal NK/T-Cell Lymphoma Using Targeted Sequencing with a Comprehensive Cancer Panel
Genomics & informatics
2016 .01
한국인의 폐선암 유전자 돌연변이: 차세대 염기서열 분석법을 이용한 검출 및 기존 유전자 검사법과의 일치도 분석
대한임상검사과학회지
2023 .03
Whole-exome sequencing analysis reveals co-segregation of a COL20A1 missense mutation in a Pakistani family with striate palmoplantar keratoderma
Genes & Genomics
2018 .01
BAG3 mutation in a patient with atypical phenotypes of myofibrillar myopathy and Charcot–Marie–Tooth disease
Genes & Genomics
2018 .01
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