Question

1. Nystagmus, a condition causing oscillations in eye movement, is inherited with the dominant allele N on the X chromosome.

0 0
Add a comment Improve this question Transcribed image text
Answer #1

he biveSeconder ie ud oile Plovo tanance of tontc nole eulog, Antesinal eiy Past mono pausal to coomen od Obesth may also

Add a comment
Know the answer?
Add Answer to:
1. Nystagmus, a condition causing oscillations in eye movement, is inherited with the dominant al...
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. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • Excess Thyroxin-binding Globulin (ETG) is a thyroid disorder that is inherited with the X-linked dominant allele...

    Excess Thyroxin-binding Globulin (ETG) is a thyroid disorder that is inherited with the X-linked dominant allele E. The X-linked recessive allele e does not contribute to ETG. Short index finger, where the index finger is shorter than the ring finger, is a sex-influenced autosomal trait that is dominant in males and recessive in females. Let allele S1 be for short index fingers and allele S2 be for long index fingers. The inheritance pattern for this trait is shown in the...

  • Vitamin D-resistant rickets is a genetic condition inherited as X-linked dominant. A husband has this Vitamin...

    Vitamin D-resistant rickets is a genetic condition inherited as X-linked dominant. A husband has this Vitamin D-resistant rickets but his wife does not. What is the probability that their first child will be a: (4 pts) a) normal son? b) normal daughter? c) son with Vitamin D-resistant rickets? d) daughter with Vitamin D-resistant rickets DHU The eye is an example of an organ that develops from a complex series of developmental events, controlled and influenced by many genes. This process...

  • 1. (2 pts) Attached ear lobes (f) are inherited as an autosomal recessive trait. The dominant...

    1. (2 pts) Attached ear lobes (f) are inherited as an autosomal recessive trait. The dominant allele, F, produces free hanging ear lobes. Sam and Beth both have free earlobes, but their first child has attached earlobes. a. What are the likely genotypes of Sam and Beth with respect to the ear lobe locus? Sam: F Beth: FF b. With respect to the earlobe locus, Sam's genotype is homozygous,/(heterozygous or hemizygous? (Circle the correct answer). c. If Sam and Beth...

  • PROBABILITY 5) In human beings, the absence of molars is inherited as a dominant trait. If two heterozygotes have f...

    PROBABILITY 5) In human beings, the absence of molars is inherited as a dominant trait. If two heterozygotes have four children, what is the probability that a.) all will have no molars? b.) three will have no molars and one will have molars? c.) the first two will have molars and the second two will have no molars? 1) Assuming a 1:1 sex ratio, what is the probability that five children produced by the same parents will consist of a.)...

  • 6. If you cross a woman with type A blood and a man with type B...

    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...

  • In this set of questions, you will need to be able to apply inheritance patterns of...

    In this set of questions, you will need to be able to apply inheritance patterns of two different characters/genes. One gene is inherited in a sex-linked pattern, while the other gene is inherited through an autosomal gene. (Answer choices include 0, 0.25, 0.5, 0.75, and 1.) In this set of questions, you will need to be able to apply inheritance patterns of two different characters/genes. One gene is inherited in a sex-linked pattern, while the other gene is inherited through...

  • 1. Examine each pedigree shown (a-c). The shaded square/circle shows an inherited phenotype. For each (a,...

    1. Examine each pedigree shown (a-c). The shaded square/circle shows an inherited phenotype. For each (a, b, c), write a sentence or two that indicates whether it is (or is not) consistent with X-linked recessive inheritance. If you decide the pedigree IS consistent, for full credit you must prove this by setting up a Punnett square or a forked line diagram. (6 pts) TO GO 2. Vitamin D-resistant rickets is a genetic condition inherited as X-linked dominant. A husband has...

  • 2. Achondroplasia is a short-limbed dwarfism that is inherited as an autosomal dominant disease. The mutant...

    2. Achondroplasia is a short-limbed dwarfism that is inherited as an autosomal dominant disease. The mutant allele that causes this form of dwarfism (D) is dominant to the normal allele at this location (d). Individuals who inherit 2 alleles for dwarfism (DD) typically have a very severe form of achondroplasia that causes extreme shortening of the bones and an underdeveloped rib cage. These individuals are usually miscarried or stillborn. Tom and Vonna both have achondroplasia (but each of them has...

  • 1. Polydactyly is a dominant trait with about 63% penetrance. A pregnant woman is heterozygous for...

    1. Polydactyly is a dominant trait with about 63% penetrance. A pregnant woman is heterozygous for the dominant allele, but does not have extra toes or fingers. Her partner does not have polydactyly and is known to be homozygous recessive for the polydactyly gene. What is the probability that their child will be born with polydactyly? 4p

  • can someone please help me with these 3 questions, thank you Scaly knuckles is a rare...

    can someone please help me with these 3 questions, thank you Scaly knuckles is a rare autosomal dominant condition in humans that is only 80% penetrant. What is the probability that a child born to a father known NOT to carry the mutation and a mother with scaly knuckles will have the condition A. 0.8 B. 0.5 C. 0.4 D. 0.2 What is the probability that a child of H and I will be affected? DO A. 1/2 B. 1/4...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT