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Klinefelter Syndrome
Inherited condition in which the affected individual is a sterile male with an XXY karyotype.
Barr Body
An inactivated X chromosome typically found in the nuclei of female mammalian cells, visible as a dense spot.
Fragile X Syndrome
A genetic disorder caused by a mutation on the X chromosome, leading to intellectual disability and physical features.
Nucleotide Triplet
A sequence of three nucleotides in DNA or RNA that codes for a specific amino acid or signifies a start or stop signal for protein synthesis.
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