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Turner Syndrome
A chromosomal disorder in females characterized by the partial or complete loss of one of the X chromosomes, leading to various developmental abnormalities.
Monosomic
A genetic condition in which an organism is missing one chromosome from a pair, leading to potential developmental abnormalities.
Genomic Imprinting
A genetic phenomenon by which certain genes are expressed in a parent-of-origin-specific manner.
Progeny
The offspring or descendants of an organism.
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