I got 0.05948 hope this helps and sorry I'm not good at explaining hopefully someone else can explain
Sexual inter course is good for health. Its like exercise. It awakens the muscles and blood pumps faster. They also say the hormones released into your brain make you smarter. Intercourse can also be bad if your partner has disease. Hope this answer helps. And don't judge me
Complete question:
You will find the complete question in the attached files, due to technical problems
Answer:
This conclusion is incorrect. Only half of the progeny will have a dominant and a recessive allele, Aa. The other half will carry two dominant alleles, AA.
Explanation:
Due to technical problems, you will find the complete explanation in the attached files.
Genotype - RR - 25%, Rr - 50%, rr - 25% (1:2:1)
Phenotype - Round seeds - 75%, Wrinkled seeds - 25% (3:1)
<h3>How explain your answer?</h3>
Let the letter "r" stand for the alleles, where R is round seeds and r is wrinkled seeds. A genotype is an individual's genes represented through alleles. Phenotypes are how the genes express themselves. In other words, genotypes will be written using letters, the alleles, and phenotypes will be the possible outcomes of the alleles.
Both of the parent seeds have the genotypes Rr and the phenotype of round seeds.
If you create punnet square (which had four boxes in total) 1 will have RR, 2 will have Rr, and 1 will have rr. These are the ratios for the genotypes. Each box represents 25%, so the percentages will be 25, 50, and 25. Finally, 3 of these boxes (RR and Rr) will result in round seeds because those are dominant. Only the genotype rr will result in wrinkled phenotype. Therefore, the ratio is 3:1 or 75% to 25%.
Thus, this could be the answer.
To learn more about genotypes and phenotypes click here:
brainly.com/question/20730322
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Answer:
The correct answer is d) genomic imprinting.
Explanation:
Genomic imprinting is a biological process by which specific modifications in the germ line that produce differences in the expression of the genetic material that is biochemically marked indicating its parental origin. The Prader-Willi syndrome is one of the best known and most studied examples in relation to pathologies produced by genomic imprinting. Prader-Willi syndrome is a complex genetic disease that is fundamentally neurological. Its appearance is due to a deletion of a fragment of chromosome 15 derived from the father.