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shutvik [7]
1 year ago
15

glucose-6-phosphate dehydrogenase deficiency (g6pd) is inherited as an x-linked recessive allele in humans. a woman whose father

suffered from g6pd marries a normal man. what proportion of their sons is expected to be g6pd?
Biology
1 answer:
Alexus [3.1K]1 year ago
6 0

0.25 of their sons is expected to be g6pd.

Because the sons will inherit only one of their mother's two X chromosomes. The father is normal, so he will pass on a normal allele. The mother has an X-linked recessive allele, so she can only pass on that allele to her daughters, who will not have G6PD deficiency.

The sons will have a 50% chance of inheriting the X chromosome from their mother—that is, they'll get either the normal or G6PD-deficient allele from her. If they get the normal allele from her, then they'll be fine and won't be affected by G6PD deficiency. If they get the G6PD-deficient allele from her, then they'll have G6PD deficiency themselves and be affected by it.

To learn more about chromosomes visit: brainly.com/question/1596925

#SPJ4

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Reagan is a young girl with a genetic developmental disorder. Her language development has been severely affected by this condit
gtnhenbr [62]

Answer:

Option D

Explanation:

Complete question

Reagan is a young girl with a genetic developmental disorder. Her language development has been severely affected by this condition, and as such she has been diagnosed with a specific language impairment. Which condition is NOT likely to have contributed to this delay?

A) autism spectrum disorder

B) Down syndrome

C) fragile-X syndrome

D) PKU

Solution

Phenylketonuria (PKU) is a kind of genetic disorder in which body starts producing and building up phenylalanine amino acid. PKU arises when the Phenylalanine hydroxylase enzyme is not synthesized due to a genetic defect thereby affecting creation of neurotransmitters such as epinephrine, norepinephrine, and dopamine. Some of the symptoms of this disorder are hyperactivity, seizures, eczema, tremors etc. PKU is not connected with language development issues and hence correct option is D

4 0
3 years ago
Part A: A scientist examines a fruit fly gene involved with the regulation of body development. A section of the DNA sequence fo
Leokris [45]

Answer:

Part A: Thr-Leu-Val

Part B: ACC-UUG-GUU

Explanation:

When you transcribe a DNA sequence to mRNA, you need to remember that in RNA there is no Thymine (T), instead it has Uracil (U). So the base pairings would be like this compared to DNA base pairing:

DNA                RNA

A-T                  A-U

T-A                  T-A

C-G                 G-C

G-C                 C-G

Given the sequence the transcription will be as follows:

DNA :   TGG - AAC - CAA  

mRNA: ACC - UUG - GUU

Next, to translate it into amino acids, you will use the chart. Now amino acids pair in codons (3 base pairs at a time).  Let's take the first codon in your sequence:

ACC

1st  2nd   3rd

 A     C       C

Using the column on the left, find the row that matches it, so in this case A.

At the very top, there is another row of letters, looking at the row of A only, look for the column of the second base which is C.

Lastly, look at the right most column and find the letter that matches the third base within the box where A and C intersect. In this case, C is your third base.

The amino acid where all three intersect is your first amino acid which is Thr.

Just do this for the next codons and you will come up with the answer.

4 0
3 years ago
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