Suppose there are four newly discovered genes, cach with two alleles, in humans that all follow a simple Mendelian inheritance pattern. Alleles are noted by a + or - for dominant and recessive, respectively. The genes and their phenotypes are listed in the table. Gene Recessive Phenotype Dominant Phenotype Wiz have the ability to cast spells cannot cast spells Serp can communicate with snakes cannot talk to snakes Time have the ability to travel through time experience normal time Drgn have the ability to hatch dormant dragon eggs cannot hatch dragon eggs What is the probability of two completely heterozygous parents having a child with a Wiz Wiz Serp Serp genotype or a child with a Wiz Wiz Serp Serp genotype? Enter your answer as a decimal.

The process by which you get a different assortment of your 4 grandparents' genes (as compared to your siblings) is called   Group of answer choices   point mutation general mutation random/independent assortment crossover effect inheritance

IN TRANSYLVANIA, SOME PEOPLE EXHIBIT TWO UNUSUAL TRAITS IN WHICH THEY HAVE VERY LONG FRONT TEETH AND THE INABILITY TO BE AWAKE WHEN THE SUN IS UP. BOTH OF THESE TRAITS APPEAR TO BE RECESSIVE. IF A WOMAN WHO IS HETEROZYGOUS FOR TEETH AND HOMOZYGOUS NORMAL FOR BEING IN THE SUN MARRIES A MAN WHO HAS BOTH THESE TRAITS, WHAT COULD BE THE PHENOTYPES AND GENOTYPES OF THEIR CHILDREN? USE A PUNNET SQUARE AND SHOW ALL WORK. LIST THE RATIOS FOR THE GENOTYPES AND PHENOTYPES.

Hereditary hemochromatosis is an autosomal recessive genetic disorder that causes the body to absorb too much iron from the diet. This excess iron is stored in the body's tissues and organs, particularly the skin, heart, liver, pancreas, and joints. Because humans cannot increase the excretion of iron, excess iron can overload and eventually damage tissues and organs. Some individuals who are homozygous for this autosomal recessive gene experience only skin discoloration and joint pain, others experience heart disease in addition to the skin discoloration, still other individuals suffer also suffer from diabetes, severe heart disease, and liver damage. Name and define this genetic phenomenon and explain how it relates to this specific genetic situation described above.

The part that is missing is where the traits for things like colorblindness and hemophilia exist. This meansthat if you have XY chromosomes, you are missing alleles on one of the chromosomes. So whatever alleleis on your X is expressed regardless of if being dominant or recessive. These X-Linked Traits have a specialway to note the alleles.X-Linked alleles use X and Y as their base and then the allele that notates the trait is in the top, rightcorner. For instance: Phenotype(appearance) Genotype(alleles) XY with Hemophilia XhY XX withouth Hemophilia XHXh Notice that the female has two X’s so has 2 alleles. She is not a hemophiliac, but is carrying the trait.That means she can pass the trait to her offspring.Why don’t you cross those two parents here and find the outcome:Parents:                                                             Offspring: Genotypes:Phenotypes:         Is there a chance of producing an XY offspring with hemophilia? Explain your answer Will…

Is the blueness a recessive trait why and why not  What was Elizabeth smith only possible genotype ? why? Why did zachry marrying his aunt cause him to have the blue sons ?

A gene has two alleles, E and e. Another gene also has two alleles, T and t. Which of the following  correctly shows linkage between the two genes? Group of answer choices ET/et Te/Et Ete/T Ee/tT

Hereditary hemochromatosis is an autosomal recessive genetic disorder that causes the body to absorb too much iron from the diet. This excess iron is stored in the body's tissues and organs, particularly the skin, heart, liver, pancreas, and joints. Because humans cannot increase the excretion of iron, excess iron can overload and eventually damage tissues and organs. A man who had hemophilia (an X-linked recessive genetic disorder), married a woman who had no family history of hemophilia whatsoever.  The couple had consulted a genetic counselor when they first contemplated having children due to concerns that their future children might have hemophilia.  Genetic testing of both future parents revealed that the husband did, in fact, possess the Hemophilia A allele but his wife was completely normal with respect to hemophilia.  Much to their shock, their first child, a daughter, had a mild blood clotting disorder.  Karyotyping was performed to determine whether this daughter had an…

Can you please not type the answer can you write it on a paper

Describe Mendel's one trait inheritance experiment examining flower color. Begin with what generation he started with and go from there. In your response, make sure to note generation names, ratios from those generations in terms of genotype and phenotype, and how did each generation come about i.e. what flowers were crossed to get the subsequent generation.