color blindness is a x linked recessive disease and it occurs usually in males as they have only X chromosomes so any mutation is expressed as compared to females who have 2 X chromsomes for them to express both of the chromosomes have to carry the mutation.
female child will be a carrier but none of the children will have colour blindness
cross is shown with only one female X chromosome as both are normal so same will happen with other one
, A woman who is normal for colour detection marries a man who is colourblind and...
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...
A woman who is heterozygous for normal vision marries a man with normal vision. If they have a girl, what is the probability she is colorblind? And what if it is a boy?
A normal woman whose father had hemophilia marries a normal man. What is the chance that they will have two children will have hemophilia? a. 100% b. 25% c. 6.25% d. 62.5% e. 0%
A color-blind woman marries a man who is not color-blind and they have six children ( 3 boys and 3 girls) All of the sons and none of the daughters are color blind. a. What does this tell you about the color blind allele? b. Draw the pedigree of this family, using correct symbols and all of the genotypes you can determine with certainty. c. One of the daughters marries a man who can see color. State the phenotypic and...
If a woman who is a carrier for sickle-cell anemia marries a man who is not a carrier, would any of their children get sickle-cell anemia? (Not sex-linked!) Prove it by doing a Punnett Square using the correct genotypes.
5. A man homozygous for a rare recessive disorder (a/a) marries a normal woman (A/A) If nondisjunction occurs in the male in meiosis I what will the gametes look like? a. b. What about if it happens in meiosis lI? 6. A man heterozygous for a rare recessive disorder (A/a) marries a normal woman (A/A) Their first child is trisomic (A/a/a) In which parent and at what stage of meiosis did nondisjunction occur? a. What kind of euploidy is this...
31. A polydactylous woman, otherwise normal, marries a healthy normal man. Their four children have the following phenotypes: (6 pt) Child 1 is normal in all respects; Child 3 has cystic fibrosis, otherwise normal Child 2 is polydactylous, otherwise normal; Child 4 has cystic fibrosis and is polydactylous. A. What is the genotype of the mother? B. What is the genotype of child 3? C. What is the genotype of child 4? D. What is the chance that child 1...
A woman marries a man with two rare, recessive X-linked alleles, a and b. Their daughter marries a normal man. What will the phenotypes of their female children be?
1. A woman with white skin has intermediate parents. If this woman marries a man with light skin, what is the darkest skin color possible for their children? The lightest? 2. A woman is color blind. What are the chances that her sons will be color-blind? If she married a man with normal vision, what are the chances that her daughters will be color blind?
A colorblind woman marries a man who is not colorblind. What is the phenotypic ratio of the offspring? In humans, freckles are dominant over absence of freckles, and curly hair is incompletely dominant with straight hair. A freckled, wavy-haired woman has kids with a freckled straight-haired man. Both the man and woman have one homozygous dominant parent and one homozygous recessive parent for freckles. What is the phenotypic ratio of the man and woman’s kids? Pigment in the mouse is...