Answer:
Incomplete dominance
Explanation:
Incomplete dominance is a type of non-mendelian inheritance pattern in which one allele of a gene is not dominant or recessive to the other allele, hence, both alleles combine to form a third intermediate phenotype, which is a blending of both parental phenotypes.
In this case, a red bird (RR) mates with a white bird (WW) to produce offsprings that have pink feathers (RW). This shows that the allele for red coloration is incompletely dominant to the allele for white coloration, hence, both combines to produce a PINK (RW) intermediate phenotype. This portrays incomplete dominance.
Sexual Reproduction with the most adapted organisms within the species
Answer:
This disorder is caused by mutations in either of two different genes; one of these genes is linked to the DNA marker locus and the other gene is not.
Explanation:
A gene marker (also known as a molecular marker) is defined as a particular DNA sequence that has a specific physical location on a given chromosome. The gene markers are always physically linked with genes of interest, thereby they are useful for identifying patients affected by a given disease and/or a particular phenotypic trait. In this case, in the first study, genetic variation of the marker has been shown to be useful to map one <em>locus</em> that is associated with the disease phenotype. However, in the second study, a second <em>locus</em> that is not linked to the marker can segregate independently, thereby showing different results from the first study (in this case, it is imperative to develop a new genetic linkage analysis to discover genetic markers linked to the second gene, which is also responsible for the disease phenotype).
Natural selection favors G6PD deficiency as compared to malaria is the best way to explain that the parasite that causes malaria doesn't survive well in G6PD-deficient cells.
Answer:
I hope this helps you
Explanation:
1)This number is abbreviated as 2n where n stands for the number of chromosomes. For humans, the diploid chromosome number equation is 2n = 46 because humans have two sets of 23 chromosomes (22 sets of two autosomal or non-sex chromosomes and one set of two sex chromosomes).
2)Under normal conditions, the haploid number is exactly half the total number of chromosomes present in the organism's somatic cells. For diploid organisms, the monoploid number and haploid number are equal; in humans, both are equal to 23.