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Explores the analysis of genotypes and variants data through a Genome-Wide Association Study, focusing on the association between genetic variants and phenotypes like height.
Explores the genetic basis of Prader-Villy syndrome and its comparison with Angelman syndrome, emphasizing DNA methylation patterns and chromosomal abnormalities.
Delves into the molecular basis of genetic diseases, discussing specific examples like Phenylketonuria and Haemophilia A, and the development of small molecule drugs for genetic disorders.
Explores the genetics of hair color, focusing on the role of the MC1R gene in determining black or red hair, and the intercellular communication involved in this process.
