Use the following information for this question: phenylketonuria is considered to be an inborn error of metabolism. it is a recessive genetic condition in which the enzyme that breaks down the amino acid phenylalanine is defective or missing. testing of all newborns allows this condition to be detected at birth. a special diet that severely minimizes phenylalanine (e. g., by avoiding diet sodas and most usual sources of protein) can treat the condition. in this scenario, two carriers of both cystic fibrosis and phenylketonuria have a child. what is the probability that the child will have cystic fibrosis and be a carrier for phenylketonuria
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Biology, 22.06.2019 01:00
Mike has a problem with his testosterone. he is unable to produce enough. which will most likely be affected by his inability to produce testosterone? check all that apply.
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Biology, 22.06.2019 01:30
Deer cave cannot support photosynthesis is as not enough sunlight is present. in spite of this, it still has a complex food chain. what is the energy foundation of this food chain?
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Biology, 22.06.2019 08:30
Both male and female gametes are created during the process of meiosis. the formation of male gametes is called spermatogenesis. after telophase il of spermatogenesis, there would be are all genetically male gametes created that
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Biology, 22.06.2019 10:00
Which is an example of a vestigial structure? a. tail of a monkey b. fin of a fish c. flower of a plant d. tailbone of a human
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Use the following information for this question: phenylketonuria is considered to be an inborn erro...
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