Question

A man who is heterozygous for the dominant condition attached earlobe has a child with a...

A man who is heterozygous for the dominant condition attached earlobe has a child with a woman who has an unattached earlobe. Their first child has an unattached earlobe. Which of the following mechanisms could explain the child's phenotype?

A.

There is no explanation needed - this is normal Mendelian inheritance

B.

Incomplete Penetrance

C.

Variable expression

D.

Incomplete dominance

Homework Answers

Answer #1

Option A

Man = Ee (attached)

Woman = ee (unattached)

Ee × ee

Gametes e
E Ee attached
e ee unattached

According to the given Four Square, a child can have either attached or attached earlobes. The probability of occurrence of both the types of hair loss is 50%. Therefore it follows a mendelian pattern of inheritance.

Incomplete dominance is the type of non mendelian inheritance in which dominant allele is in completely dominant over the recessive allele and therefore heterozygotes show intermediate phenotype.

Please give a good rating.

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
Using a graph/Punnett square: A woman is heterozygous for polydactyly (which is a dominant condition in...
Using a graph/Punnett square: A woman is heterozygous for polydactyly (which is a dominant condition in which a person has more than the normal number of fingers and/or toes). The woman has a child with a man who is homozygous normal. What is the chance that their child will have more than ten fingers and/or toes?
2. Crossing over occurs in mitosis Neither mitosis nor meiosis Both mitosis and meiosis meiosis 3....
2. Crossing over occurs in mitosis Neither mitosis nor meiosis Both mitosis and meiosis meiosis 3. Given that E=unattached earlobes and e=attached earlobes what is the phenotype of an individual who is heterozygous for earlobe attachment? attached earlobes unattached earlobes one attached and one unattached earlobe. EE 4. Given that E=unattached earlobes and e=attached earlobes, what is the genotype of an individual who is heterozygous for earlobe attachment? Unattached earlobe ee Ee EF 5. With regards to X linked recessive...
Widow’s Peak is dominant to not having it. A woman who has widow’s peack marries a...
Widow’s Peak is dominant to not having it. A woman who has widow’s peack marries a man who doesn’t. Their first child has his father's phenotype. What are the chances that their second child will have widow’s peak and be a girl?
Having freckles is a dominant trait. A person is heterozygous for having freckles. Their genotype is...
Having freckles is a dominant trait. A person is heterozygous for having freckles. Their genotype is _________ and their phenotype is _________. [ Choose the choice with the answers in the correct order. ] * Freckles, Ff ff, freckles freckles, no freckles Ff, Freckles A fertilized egg created through sexual reproduction ______________. * is genetically identical to the parents contains genetic material from only one parent is genetically identical to other eggs of the same parents has a combination of...
An autosomal dominant condition causes deafness in people. However, 40% of people who are known to...
An autosomal dominant condition causes deafness in people. However, 40% of people who are known to have at least one copy of the dominant allele have normal hearing (no deafness). Additionally, the severity of deafness varies between individuals with the condition. Some people have complete deafness, some people moderate deafness, and some people only have mild deafness. The occurrence or not of deafness in people who have at least one dominant allele is an example of: Codominance Epistasis Expressivity Penetrance...
Color blindness in humans is recessive. A heterozygous man and a woman who is homozygous for...
Color blindness in humans is recessive. A heterozygous man and a woman who is homozygous for color blindness decide to raise a family of 3 children. a) What is the probability that 2 of the children have normal vision, and 1 are color blind? b) What is the probability that 1 of the children has normal vision, and 2 are color blind? c) What is the probability that all of the children are color blind? d) What is the probability...
A man and woman both have one parent who has albinism but both (man and woman...
A man and woman both have one parent who has albinism but both (man and woman ) have normal skin pigmentation. What is the probability that their first child will have albinism if albinism is a recessive trait?
A mother has blood type AB and a father has blood type O and they have...
A mother has blood type AB and a father has blood type O and they have a child together. 8. If blood is needed to be given to the mother and AB blood type is not available, what other blood type(s) can the mother receive (not considering Rh factor)? Explain your answer. 9. Explain why a person with AO genotype has the same phenotype (blood type A) as a person with AA genotype. Pink is the phenotype from the expression...
A man with hemophilia (a recessive, sex-linked condition) and a woman that carries the hemophilia allele...
A man with hemophilia (a recessive, sex-linked condition) and a woman that carries the hemophilia allele have a daughter with normal phenotype. Define allele symbols for the hemophilia and normal alleles. Draw a pedigree and indicate the genotype of each individual in the pedigree. The daughter marries a man who is normal for the trait. What is the probability that a daughter of this pair will be a hemophiliac? What is the probability that a son will be a hemophiliac?...
A woman (Tina) has a certain genetic condition (is affected). She goes to a genetic counselor...
A woman (Tina) has a certain genetic condition (is affected). She goes to a genetic counselor to learn about the inheritance pattern of the condition and to ascertain the chance that she might pass it to her offspring. The following is the information she gives the Genetic Counselor. (assume that this condition displays 100% penetrance, results from a single genetic mutation and exhibits complete dominance) 1) Tina is the fourth born of seven children. Her oldest sibling is an affected...
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT