Answer:
The correct statement that explains why none of Queen Victoria’s daughters had hemophilia is: Females with hemophilia must inherit the gene from both parents to be affected.
Hemophilia is a sex-linked recessive disorder, which means it is located on the X chromosome. Males have one X chromosome and one Y chromosome, while females have two X chromosomes. A male who inherits a hemophilia gene on his X chromosome from his mother will have the condition because he does not have a second X chromosome to mask the effects of the gene. However, a female who inherits a hemophilia gene on one X chromosome will not have the condition if her other X chromosome has a normal gene that masks the effects of the hemophilia gene. In other words, a female with only one hemophilia gene is a carrier of the disorder but does not express it.
Therefore, Queen Victoria's daughters, who received one X chromosome from their mother (who was a carrier of the hemophilia gene) and one X chromosome from their father (who did not have the hemophilia gene), did not have hemophilia because they inherited the normal gene from their father that masked the hemophilia gene from their mother.
Step-by-step explanation:
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