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valentinak56 [21]
2 years ago
8

Patel and her siblings try to stick to a low salt diet since they have inherited high blood pressure from their mother. This is

a great solution to overcome which health determinant?
Biology and genetics
Family and cultural influences
Health services
Social and physical factors
Biology
1 answer:
garri49 [273]2 years ago
6 0

The low salt diet is a great solution to overcome heath determinant of Biology and genetics.

  • According to this question, Patel and her siblings have inherited high blood pressure from their parents. This tells us that the health condition is a genetic disorder, which is branch of Biology.

  • Patel and her siblings are however, on a low salt diet as a solution to overcome the health challenge (high blood pressure).

This solution is, hence, a great solution to overcome the heath determinant of Biology and genetics.

Learn more: brainly.com/question/12138821?referrer=searchResults

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Brrunno [24]

Answer:

d.0.48

Explanation:

When a population is in Hardy Weinberg equilibrium the <u>genotypic </u>frequencies are:

freq (AA) = p²

freq (Aa) = 2pq

freq (aa) = q²

<em>p</em> is the frequency of the dominant <em>A</em> allele and <em>q</em> is the frequency of the recessive <em>a</em> allele.

In this population of 100 individuals, 84 martians have the dominant phenotype and 16 have the recessive phenotype.

Therefore:

q²=16/100

q² = 0.16

q=√0.16

q = 0.4

And p+q=1, so:

p = 1 - q

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p = 0.6

The frequency of heterozygotes is:

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5 0
3 years ago
Which mutations is most likely to cause a phenotypic change?
melomori [17]

The question is incomplete. The complete question is as follows:

Which of the following mutations is most likely to cause a phenotypic change?

A) a duplication of all or most introns

B) a large inversion whose ends are each in intergenic regions

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D) a single nucleotide deletion in an exon coding for an active site

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Explanation:

Deletion or insertion of a single nucleotide in an axon coding for an active site is called frameshift mutation.

The sequence of codons is read during translation, in order to synthesize a amino acids chain and form a protein from the nucleotide sequence. Frameshift mutations occur when the usual codon sequence is broken by the deletion or addition of one or more nucleotides. For example, if only one nucleotide is removed from the axon sequence during the RNA splicing process, then there will be a disrupted reading frame for all codons before and after the mutation. This may result in several incorrect amino acids being introduced into the protein. Disruption in protein sequence will cause phenotypic change.

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Answer:

i have trusted my best to answer

Explanation:

Edit

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