Biology: The Unity and Diversity of Life (MindTap Course List)
15th Edition
ISBN: 9781337408332
Author: Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 13, Problem 1SQ
Summary Introduction
Concept introduction: The pair of chromosome where one of the pair is of maternal source and the other is of paternal source that has genes in the same loci with variable alleles of the gene is called as homologous chromosomes. Allele is the modification of the gene. Alleles are of two types namely dominant and recessive.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Retinitis pigmentosa, a form of blindness in man, maybe caused either by a dominant autosomal gene R, or a recessive autosomal gene a. An afflicted man whose parents are both normal marries a woman with genotype AaRr. a. What proportion of the children are expected to suffer from this affliction if R and A are inherited independently?
b. If this couple want to have normal children only, what isthe probability of having normal children?
Webbed fingers is inherited as an X-linked disease An unaffected male marries an
affected female.
a. Draw a Punnett square of the possible offspring.
b. List the phenotypes of the possible children
c. Draw a pedigree that displays the inheritance in you Punnett square
Independent assortment means thata. two genes tend to be inherited together.b. which allele of a gene is included in a gamete has noeffect on which allele of a second gene is included in thesame gamete.c. which allele of a gene is included in a gametedetermines which allele of a second gene is included inthe same gamete.d. homologous chromosomes do not separate during meiosis.
Chapter 13 Solutions
Biology: The Unity and Diversity of Life (MindTap Course List)
Ch. 13 - Prob. 1DAACh. 13 - Prob. 2DAACh. 13 - Prob. 3DAACh. 13 - Prob. 1SQCh. 13 - An organisms observable traits constitute its...Ch. 13 - Prob. 3SQCh. 13 - Prob. 4SQCh. 13 - The offspring of the cross AA aa are ________. a....Ch. 13 - Refer to question 5. Assuming complete dominance,...Ch. 13 - A testcross is a way to determine ________. a....
Ch. 13 - Assuming complete dominance, a cross between...Ch. 13 - The probability of a crossover occurring between...Ch. 13 - True or false? All traits are inherited in a...Ch. 13 - One gene that affects three traits is an example...Ch. 13 - The phenotype of individuals heterozygous for...Ch. 13 - _______ in a trait is indicated by a bell curve....Ch. 13 - Match the terms with the best description. ______...Ch. 13 - Mendel crossed a true-breeding pea plant with...Ch. 13 - Assuming that independent assortment occurs during...Ch. 13 - Refer to problem 2. Determine the predicted...Ch. 13 - For each genotype listed, what allele combinations...Ch. 13 - Prob. 5GPCh. 13 - Suppose you identify a new gene in mice. One of...Ch. 13 - Mutations in the TYR gene may render its enzyme...Ch. 13 - In sweet pea plants, an allele for purple flowers....Ch. 13 - Red-flowering snapdragons are homozygous for...
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- A heterozygous individual has _______ for a trait being studied. a. the same allele on both homologous chromosomes b. two different alleles of a gene c. a haploid condition, in genetic termsarrow_forwardAlleles for Tay-Sachs disease are inherited in an autosomal recessive pattern. Why would two parents with a normal phenotype have a child with Tay-Sachs? a. Both parents are homozygous for a Tay-Sachs allele. b. Both parents are heterozygous for a Tay-Sachs allele. c. New mutations gave rise to Tay-Sachs in the child. d. b or carrow_forwardThe F1 flies described in question 1 were mated with brown-eyed flies from a true-breeding line. What phenotypes would you expect the offspring to have? (a) all with red eyes (b) all with brown eyes (c) half with red eyes and half with brown eyes (d) red-eyed females and brown-eyed males (e) brown-eyed females and red-eyed malesarrow_forward
- Cystic fibrosis is an autosomal disease that mainly affects the white population, and 1 in 20 whites are heterozygotes. Genetic testing can diagnose heterozygotes. Should a genetic screening program for cystic fibrosis be instituted? Should the federal government fund it? Should the program be voluntary or mandatory, and why?arrow_forwardTay–Sachs disease is caused by recessive alleles on anautosome. In which case(s) could two parents with anormal phenotype have a child with Tay–Sachs?a. Both parents are homozygous for a Tay–Sachs allele.b. Both parents are heterozygous for a Tay–Sachsallele.c. One parent is homozygous for a Tay–Sachs allele,and the other is heterozygous.arrow_forwardChromosomes undergo division during meiosis. Such chromosomal behaviors are consistent with Mendel's laws of a. Unit Characters b. None of these c. Dominance and Recessiveness d. Independent Assortment e. Secondary Nondisjunction Chromosomes undergo division during meiosis. Such chromosomal behaviors are consistent with Mendel's laws of a. Unit Characters b. None of these c. Dominance and Recessiveness d. Independent Assortment e. Secondary Nondisjunctionarrow_forward
- Please explain I don’t think this is autosomal dominant as female are more affected than male and please explain B part of the question well.arrow_forwardA single syndrome that has more than one genetic causeexhibits ________.a. pleiotropyb. incomplete penetrancec. genetic heterogeneityd. variable expressivityarrow_forwardMany genetic disorders are inherited in a recessive manner Select one: a. False b. Truearrow_forward
- Hemophilia is a disease caused by a gene found on the X chromosome. Therefore, it is referred to as a sex-linked disease. The recessive allele causes the disease. A man with hemophilia (xhy) marries a woman who is homozygous dominant (XHXH. A. Illustrate using a Punnett square the probability that their children will have the disease. B. Will any of their children have the disease? C. Predict the probabilities of their children having the disease.arrow_forwardThe flower color gene studied by Mendel affected three traits. This is an example of ________. a. pleiotropic genes b. codominant inheritance c. polygenic inheritancearrow_forwardA trait that is present in a male child but not in either of his parents is characteristic of inheritance. a. autosomal dominant b. autosomal recessive c. X-linked recessive d. It is impossible to answer this question without more informationarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Biology Today and Tomorrow without Physiology (Mi...BiologyISBN:9781305117396Author:Cecie Starr, Christine Evers, Lisa StarrPublisher:Cengage Learning
Biology (MindTap Course List)BiologyISBN:9781337392938Author:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. BergPublisher:Cengage Learning
Human Heredity: Principles and Issues (MindTap Co...BiologyISBN:9781305251052Author:Michael CummingsPublisher:Cengage Learning
Biology Today and Tomorrow without Physiology (Mi...
Biology
ISBN:9781305117396
Author:Cecie Starr, Christine Evers, Lisa Starr
Publisher:Cengage Learning
Biology (MindTap Course List)
Biology
ISBN:9781337392938
Author:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg
Publisher:Cengage Learning
Human Heredity: Principles and Issues (MindTap Co...
Biology
ISBN:9781305251052
Author:Michael Cummings
Publisher:Cengage Learning
How to solve genetics probability problems; Author: Shomu's Biology;https://www.youtube.com/watch?v=R0yjfb1ooUs;License: Standard YouTube License, CC-BY
Beyond Mendelian Genetics: Complex Patterns of Inheritance; Author: Professor Dave Explains;https://www.youtube.com/watch?v=-EmvmBuK-B8;License: Standard YouTube License, CC-BY