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Inactivated X Chromosome
Also known as the Barr Body; a dense body formed from a deactivated X chromosome found in the nuclei of female cells, ensuring dosage compensation between males and females.
Heterozygous
Having two different alleles of a gene, one inherited from each parent, resulting in genetic variation.
Hemophilia
A genetic disorder leading to impaired blood clotting, resulting from deficiency or dysfunction of clotting factors.
Punnett Square
A diagram used in genetics to predict the genotypic and phenotypic outcomes of a particular cross or breeding experiment.
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