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pshichka [43]
3 years ago
14

Galactosemia is an inherited disorder in humans a person with the disorder cannot digest the sugars in the allelebfor normal dig

estion (G) is dominant the allele for (g) is recessive a female who is heterozygous for the galactosemia trait and a male who has galactosemia have a child
Biology
1 answer:
Elanso [62]3 years ago
4 0
The Genotype of the father is gg; The possible genotypes of offspring will be 
Gg; gg; Gg; gg. Therefore there is a 50% chance that the child will have galactosemia. The parents could have had; both had gg genotype,or both had Gg genotype, or one had gg and the other Gg.
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Answer:

See explanation below.

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<em>Study Design - Partially double-blinded study</em>

  • The <u>cohort study </u>will be composed of 80 adults (aged ≥18 years) with a clinical diagnosis of constant coughing present as a result of a cold, which would be measured by semiautomated ambulatory cough monitor.
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Participant cough will be recorded <u>every hour</u> (until 8 hours are reached) for two consecutive days (for repetitions) in both groups using semiautomated ambulatory cough monitor and analyzed statistically.

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*<em>In scientific experiments, repetitions are important to prevent bias and error.</em>

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