since Margaret's father is affected with the disease she is heterozygous for the trait, let the affected allele be Xh and normal allele be XH then Margaret is XHXh and her husband Mark is not hemophilic so he is XHY.
A) XHXh*XHY
| XH | Xh | |
| XH | XHXH (normal female) | XHXh (carrier female) |
| Y | XHY (normal male ) | XhY (affected male) |
probability of that girl is affected = number of affected girls/ number of girls=0/2=0
B) probability that boy is affected= number of affected boys/ number of boys=1/2
C) probability of that all 3 boys are affected= (probability of boy is affected)^4=(1/2)^4=1/16
D) Daughter can be either normal female or carrier female if the daughter is a normal female then all of her daughters will have at least one copy of normal allele so daughters are not affected but when the female is carrier XHXh*XhY
| XH | Xh | |
| Xh | XHXh | XhXh (affected female) |
| Y | XHY | XhY |
the probability that daughter is affected = number of affected girls/total number=1/2
E)Daughter can be either a normal female or carrier female if the daughter is a normal female then all of her sons will get a normal allele so no sons are affected. but when the female is carrier XHXh*XhY
(from above punnet square )
the probability that boy is affected the = number of affected boy/number of boys=1/2
4. [15 pts total] Sam has hemophilia (a recessive, X-linked condition) but his daughter Margaret has...
Hemophilia in humans is a recessive sex-linked trait. A man with hemophilia and a woman who does not have hemophilia have a daughter who does not have hemophilia. She then marries a man who does not have hemophilia. What is the probability that their first child will be a daughter with hemophilia? A daughter without hemophilia? A son with hemophilia? A son without hemophilia? If the couple has four sons, what is the probability that all four will be born...
Hemophilia is a sex-linked X-linked recessive trait. A homozygous normal woman marries a normal man whose brother has hemophilia. What are the chances of them having a hemophiliac son; hemophiliac daughter?
DO EITHER QUESTION 11 OR QUESTION 12. NOT BOTH. We will only mark Question 11 if it is not clear which one you attempted. 11) Hemophilla is a sex-linked trait. A normal woman marries a normal man and they have 1 daughter and 2 sons. One son has hemophilia but the other two are normal. The normal daughter marries a hemophiliac man and they have2 sons and 2 daughters. One son and one daughter have hemophilia but other 2 children...
Hemophilia B is an X-linked recessive trait that causes problems with blood-clotting. (2 pts) If a normal man and a woman who is a carrier for hemophila decide to have children, what is the probability their first child will have hemophila? Please show your work using a Punnett Square. (3 pts) How would X inactivation in the woman described above (a carrier for hemophilia) affect her phenotype for hemophilia symptoms?
6. If you cross a woman with type A blood and a man with type B and both ha dominant and one recessive allele for blood type what are the possible genotypes of their offspring? Use the Punnett square below to help you determin etermine this. 7. Choroideremia is a disease that causes degeneration of the retina of the eye. The recessive allele that causes this condition is found on the X chromosome. Using the square below, cross a woman...
A certain type of hemophilia is X-linked recessive in humans. A woman has this disease and has children with a man who has normal blood clotting (no hemophilia). All their [ Select ] ["sons", "daughters", "children (regardless of their sex)"] will have hemophilia.
3. Colour-blindness is a X-linked, recessive trait. If a normal-sighted woman, whose father was colour-blind, marries a colour-blind man, what is the probability that they will have a son who is colour-blind? (use the letter "B") 4. A man and woman, both of normal vision, have: 1) a colour-blind son (#1) who has a daughter of normal vision 2) a daughter (#1) of normal vision who has one colour-blind son and one normal vision son 3) another daughter (W2) of...
Hemophilia is an X linked recessive condition in humans (Xh). Blood type (AB) is determined utilizing multiple alleles of I, two of which are codominant. A widow's peak is determined by a single dominant allele (W), while the recessive phenotype is a straight hairline. The ability to taste PTC is determined by a single dominant allele (T). while the recessive phenotype is a non-taster. Eugene is a non-taster male who does not have hemophilia. He has AB blood and a...
need help with 1 and 2 please.
X-linked Recessive Traits Review X-linked traits in your textbook. 1 In cars, the Ballele produces black fur & b produces orange fur. This gene is X-linked (X & X". Both colors are expressed in heterozygotes calico). If alcat has 2 calico kittens, 1 male black kitten, and I female orange kitten, what is the ty p henotype of the father cat? (Hint: Work backwards & use a Punnett square Remember that not every...
1. For each of the following blood types, list the possible genotypes: Phenotype Possible Genotypes A B AB O 2. Dr. Paul is blood type O. His father was blood type A and his mother was blood type B. What were the genotypes of his parents? What are the possible blood types and phenotypic ratios expected for a cross involving these parental genotypes? 3. In the ABO blood system in human beings, alleles A and B are codominant and both are...