What are the two tiny structures located in the cytoplasm near the nuclear envelope at the beginning of prophase?
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Answer:
The female (XcX) is carrier for color blindness while the male (XY) is normal. The carrier female transmits its one X chromosome with gene for color blindness to one of her sons making him color blind.
Explanation:
Color blindness is X linked recessive disorder and followed the criss-cross inheritance wherein the color blind sons get the gene from their carrier/affected mother while the color blind father would transmit the gene to his daughters along with X chromosome.
Since both the parents are normal, the mother (XcX) should be carrier for the disease to get the color blind son. A cross between carrier mother (XcX) and normal father (XY) would make 50% of their sons color blind.
