A woman that is heterozygous for neurofibromatosis and a normal man (homozygous recessive for neurofibromatosis) will exhibit a 1:1 phenotype ratio in offspring (Option d).
<h3>What is a rare dominant autosomal genetic disease?</h3>
A rare dominant autosomal genetic disease is a condition inherited in a dominant pattern in very low frequency in the population.
Dominant autosomal genetic diseases are expressed in a 1:1 ratio because they are localized in autosomal (somatic) chromosomes instead of X and Y chromosomes.
In conclusion, a woman that is heterozygous for neurofibromatosis and a normal man (homozygous recessive for neurofibromatosis) will exhibit a 1:1 phenotype ratio in offspring (Option d).
Learn more about dominant autosomal genetic diseases here:
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Answer: Glucose is absorbed through the intestine by a transepithelial transport system initiated at the apical membrane by the cotransporter
Explanation:
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Heredity increases diversity because when we inherit traits from our parents, we become a mix of both. Then, when we have children, they will inherit some of our traits and some of the other parent's traits. That increases diversity because different people get mixed together and create a new kind of person.
Answer:
The purpose of the Green Revolution was to
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