Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing

Keyphrases

• Next-generation Sequencing 100%
• Sequence Variants 100%
• Nonsyndromic 100%
• Premature Ovarian Failure 100%
• Genetic Linkage Analysis 100%
• Coding Sequence 100%
• Etiology 12%
• Syndromic 12%
• Genomic Regions 12%
• Physicochemical Properties 12%
• Sanger Sequencing 12%
• 40 Years Old 12%
• Sequence Variation 12%
• Genetic Origin 12%
• Molecular Complexity 12%
• Reproductive Phenotype 12%
• Coding mutation 12%
• Human Infertility 12%
• Failure Cases 12%
• Molecular Effects 12%
• Under 40 12%
• Quantitative Traits 12%
• Genetic Anomalies 12%
• Amino Acid Substitution 12%
• Functional Test 12%
• Multifunctional Protein 12%
• X-linked 12%
• Coding Variants 12%
• Non-synonymous mutation 12%
• Compensatory Effect 12%
• Subtle Interaction 12%
• Gene-based 12%
• Mammalian Reproduction 12%
• Restricted numbers 12%
• Functional SNP 12%
• Pathological Phenotype 12%
• Hypergonadotropic 12%
• Cellular Effects 12%

Biochemistry, Genetics and Molecular Biology

• Genetics 100%
• Next Generation Sequencing 100%
• Genetic Linkage Analysis 100%
• Candidate Gene 50%
• Genomics 50%
• Dideoxynucleotide Sequencing 50%
• Single Nucleotide Polymorphism 50%
• Quantitative Trait 50%
• Amino Acid Substitution 50%
• Functional Property of Proteins 50%

Medicine and Dentistry

• Linkage Analysis 100%
• Next Generation Sequencing 100%
• Primary Ovarian Insufficiency 100%
• Genetic Linkage 100%
• Diseases 25%
• Reproductive Medicine 25%
• Sanger Sequencing 12%
• Single Nucleotide Polymorphism 12%
• Functional Property of Proteins 12%
• Amino Acid Substitution 12%