Maria has classic hemophilia, an x-linked recessive disease. Could Maria have inherited the gene for this...
Maria has classic hemophilia, an x-linked recessive disease. Could Maria have inherited the gene for this disease from the following persons? Yes or No?
(a) her father
(b) her mother's father
(c) her father's father
(d) her mother's mother
(e) her mother
(f) her father's mother
Homework Answers
I believe the correct answer to be:
A) Yes
B) Yes
C) No
D) Yes
E) Yes
F) Yes
feel free to leave a comment down below for any further query. good rating would be appreciated if you find my answer helpful. thank you.
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Maria has classic hemophilia, an x-linked recessive disease.
Could Maria have inherited the gene for this...
need help with 1 and 2 please. X-linked Recessive Traits Review X-linked traits in your textbook....
need help with 1 and 2 please.
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Colorblindness and Hemophilia A are X-linked recessive conditions. A woman heterozygous for hemophila mutation and a...
Colorblindness and Hemophilia A are X-linked recessive conditions. A woman heterozygous for hemophila mutation and a colorblind man have a son who is haemophilic and has Klinefelter's syndrome (XXY). Which of the following nondisjunction events is the most compatible with the situation described? Please provide an explanation a. meiosis I, mother b. meiosis II, mother c. meiosis I, father d. meiosis II, father e. a and b
Questions of Question 50 2.5 points Save A Hemophilia is inherited as an X-linked recessive mutation....
Questions of Question 50 2.5 points Save A Hemophilia is inherited as an X-linked recessive mutation. Tay Sachs disease (ts) is inherited as an autosomal recessive. A hemophilic man is heterozygous for the sale. What fraction of his sperm will carry the recessivets allele and the hemophilia allele together? 1/8 12 14 176
A certain type of hemophilia is X-linked recessive in humans. A woman has this disease and...
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.
Two normal parents have a son with hemophilia (an X-linked recessive disorder) that also has Klinefelter...
Two normal parents have a son with hemophilia (an X-linked recessive disorder) that also has Klinefelter Syndrome. a. Write out the cross as described above illustrating the genotypes and phenotypes of the parents and child. b. Did the non-disjunction event occur in the mother, the father, or could have occurred in either of the two parents? c. Did the nondisjunction event occur during meiosis I, meiosis II, or could it have occurred in either division during meiosis.
3. (35 pts) The gene for the cone photoreceptor in the eye and the gene for...
3. (35 pts) The gene for the cone photoreceptor in the eye and the gene for a blood-clotting factor are both in the X-chromosome. Suppose they are 14 map units apart. Mutation in the photoreceptor gene results in color blindness, and is inherited as an X-linked recessive trait. Mutation in the clotting factor gene results in hemophilia, and is also inherited as an X-linked recessive trait. You have two patients: Sally and Jill. Both patients have a family history of...
Two normal parents have a daughter with hemophilia (an X-linked recessive disorder) that also has Turner...
Two normal parents have a daughter with hemophilia (an X-linked recessive disorder) that also has Turner Syndrome. a. Write out the cross as described above illustrating the genotypes and phenotypes of the parents and child. b. Did the non-disjunction event occur in the mother, the father, or could have occurred in either of the two parents? Did the nondisjunction event occur during meiosis I, meiosis II, or could it have occurred in either division during meiosis.
A woman with albinism (an X-linked recessive gene) has a child with a man who has...
A woman with albinism (an X-linked recessive gene) has a child with a man who has normal pigment. Their child has albinism with Klinefelter's syndrome (XXY). Where did the non-disjunction event occur? a.Could only have occurred in the mother b.Can't determine from the information given. c.Could only have occurred in the father d.Could have occurred in either the mother or the father
Hemophilia is an x-linked recessive trait. In a population of 2000 people, 4 women have hemophilia,...
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A woman with the recessive, X-linked disorder hemophilia has children with a male who is color-blind,...
A woman with the recessive, X-linked disorder hemophilia has children with a male who is color-blind, also a recessive X-linked disorder. What is the probability that their children will have hemophilia and have normal vision? a. 0 b. 1/4 c. 1/2 d. 3/4 e. 1
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...
Questions of Question 50 2.5 points Save A Hemophilia is inherited as an X-linked recessive mutation. Tay Sachs disease (ts) is inherited as an autosomal recessive. A hemophilic man is heterozygous for the sale. What fraction of his sperm will carry the recessivets allele and the hemophilia allele together? 1/8 12 14 176
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