4. The couple shown by the pedigree shown below, have 2 children, 1 girl with the disease and 1 boy without the disease as shown. What is the mode of inheritance? (is the disease autosomai recessive, autosomal dominant, or X-linked recessive?) Explain why you think this. Fill in the genotypes to help you answer this.

4. The couple shown by the pedigree shown below, have 2 children, 1 girl with the disease and 1 boy without the disease as shown. What is the mode of inheritance? (is the disease autosomai recessive, autosomal dominant, or X-linked recessive?) Explain why you think this. Fill in the genotypes to help you answer this.

Name: 4. The couple shown by the pedigree shown below, have 2 children, 1 g
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Description: 4. The couple shown by the pedigree shown below, have 2 children, 1 girl with the disease and 1 boy withoutthe disease as shown. What is the mode of inheritance? (is the disease autosomal recessive, autosomaldominant, or X-linked recessive?) Explain

Biology (MindTap Course List)

11th Edition

ISBN:9781337392938

Author:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg

Publisher:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg

Chapter16: Human Genetics And The Human Genome

Section: Chapter Questions

Problem 8TYU

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Similar questions

The following pedigree shows the pattern of inheritance of red green color blindness in a family. Females are shown as circles and males as squares; the squares or circles of individuals affected by the trait are filled in red. What is the chance that a son of the third-generation female indicated by the arrow will be color-blind if the father is a normal man? If the father is color-blind?
Choose the statement that is incorrect. a. A son can inherit a recessive allele on an X chromosome from either parent. b. An individual may inherit three or more of each type of chromosome characteristic or the species, a condition called polyploidy. c. A female child inherits one X chromosome from her mother and one from her father. d. Pedigree analysis can be used to determine a future childs chance of being born with achcondroplasia.
A heterozygous individual has a _______ for a trait being studied. a. pair of identical alleles b. pair of nonidentical alleles c. haploid condition, in genetic terms
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