Identification of mutations in the human EXT₁ and EXT₂ genes

Keyphrases

• Exostosis 100%
• EXT1 Gene 100%
• EXT2 Gene 100%
• Genetic Basis 20%
• Disease Diagnosis 20%
• Tumor Suppressor Gene 20%
• Chromosome 11 20%
• Coding Region 20%
• Exon 6 20%
• Genetic Counseling 20%
• Chromosome 8 20%
• Frameshift 20%
• Premature Termination 20%
• Bone Disorders 20%
• Frameshift mutation 20%
• Exon 2 20%
• Hereditary multiple Exostoses 20%
• PCR-SSCP 20%
• Prenatal Genetic Testing 20%
• Gene Diagnosis 20%

Biochemistry, Genetics and Molecular Biology

• EXT1 100%
• EXT2 (Gene) 100%
• Exon 66%
• Single-Strand Conformation Polymorphism 33%
• Frameshift Mutation 33%
• Genetic Prenatal Diagnosis 33%
• Genetics 33%
• Genetic Counseling 33%
• Tumor Suppressor Gene 33%
• Chromosome 11 33%
• Coding Region 33%
• Chromosome 8 33%
• Hereditary Multiple Exostosis 33%
• Polymerase Chain Reaction 33%