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X Chromosome Inactivation
A process in female mammals where one of the two X chromosomes is inactivated to ensure dosage compensation for gender-based genetic differences.
Phenotype
The set of observable characteristics of an individual resulting from the interaction of its genotype with the environment.
Homozygous
A genetic condition where an individual inherits the same alleles for a particular gene from both parents.
Heterozygous
Having two different alleles of a particular gene or genes, resulting in a variation in a specific genetic trait.
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