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Multiple Choice
Females who have one abnormal copy of a mutated gene on the X chromosome are known as:
A
hemizygotes
B
carriers
C
homozygotes
D
affected individuals
Verified step by step guidance
1
Understand the genetic context: Females have two X chromosomes, so they have two copies of genes located on the X chromosome.
Define the term 'hemizygote': This refers to individuals (usually males) who have only one copy of a gene on the X chromosome because they have one X and one Y chromosome.
Define 'homozygote': This refers to individuals who have two identical alleles of a gene, either both normal or both mutated.
Define 'affected individuals': These are individuals who express the disease phenotype, often because they have two mutated copies or a mutation on their single X chromosome (in males).
Recognize that females with one mutated and one normal copy of an X-linked gene typically do not show full disease symptoms but can pass the mutation to offspring; such females are called 'carriers'.