Principles of Biology
2nd Edition
ISBN: 9781259875120
Author: Robert Brooker, Eric P. Widmaier Dr., Linda Graham Dr. Ph.D., Peter Stiling Dr. Ph.D.
Publisher: McGraw-Hill Education
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Chapter 14.4, Problem 3TYK
Summary Introduction
Introduction:
Down syndrome is a condition, in which the development of the affected person is declined, which result in physical and mental abnormalities. It is caused be the presence of an extra 21 chromosome.
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A misaligned crossover between two homologous chromosomes usually results in:
A phenotypically normal individual has the following combinations of normal and abnormal chromosomes:The normal chromosomes are shown on the left in each pair.Suggest a series of events (breaks, translocations, crossovers, etc.)that may have produced this combination of chromosomes.
The inactivation of one of the X chromosomes forms a structure known as a(n):
telomere
centromere
autosome
Barr body
A man who carries a dominant X-linked trait will pass this trait on to:
all of his sons
all of his daughters
half of his daughters and half of his sons
half of his daughters
An individual possessing two copies of the same sex chromosomes is known as:
Question 3 options:
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homogametic
Chapter 14 Solutions
Principles of Biology
Ch. 14.1 - Researchers usually treat cells with drugs that...Ch. 14.1 - Researchers usually treat cells with drugs that...Ch. 14.1 - Refer back to Figure 13.13. How do checkpoint...Ch. 14.1 - A cell that is diploid has two chromosomes. pairs...Ch. 14.1 - In eukaryotes, DNA replication produces sister...Ch. 14.1 - Prob. 3TYKCh. 14.2 - Refer back to the karyotype in Figure 14.1. In...Ch. 14.2 - What are the functions of the three types of...Ch. 14.2 - Prob. 1TYKCh. 14.2 - Prob. 2TYK
Ch. 14.2 - Sister chromatids separate from each other during...Ch. 14.2 - With regard to chromosome composition, how does...Ch. 14.3 - Prob. 1CCCh. 14.3 - Prob. 2CCCh. 14.3 - What is the main reason for meiosis in animals?...Ch. 14.3 - In meiosis I, crossing over occurs during...Ch. 14.3 - Prob. 2TYKCh. 14.3 - Prob. 3TYKCh. 14.4 - Prob. 1CCCh. 14.4 - A chromosome in which the telomere is at one end...Ch. 14.4 - Prob. 2TYKCh. 14.4 - Prob. 3TYKCh. 14 - Prob. 1TYCh. 14 - Prob. 2TYCh. 14 - Checkpoints during the cell cycle are important...Ch. 14 - Prob. 4TYCh. 14 - Prob. 5TYCh. 14 - Prob. 6TYCh. 14 - Prob. 7TYCh. 14 - Prob. 8TYCh. 14 - Prob. 9TYCh. 14 - Prob. 10TYCh. 14 - Distinguish between homologous chromosomes and...Ch. 14 - The Oca2 gene, which influences eye color in...Ch. 14 - PRINCIPLES A principle of biology is that cells...Ch. 14 - Why is it necessary for chromosomes to condense...
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- Given that a human normally contains 46 chromosomes, give the chromosome number for each of the following conditions: Turner syndrome (female, no Barr bodies): Klinefelter syndrome (male, one Barr body): Triploid: Down syndrome (trisomic): Trisomy 13:arrow_forwardMen have XY (or YX) chromosomes and women have XX chromosomes. X-linked recessive genetic diseases (such as juvenile retinoschisis) occur when there is a defective X chromosome that occurs without a paired X chromosome that is not defective. Represent a defective X chromosome with lowercase x, so a child with the xY or Yx pair of chromosomes will have the disease and a child with XX or XY or YX or xX or Xx will not have the disease. Each parent contributes one of the chromosomes to the child. Complete parts a through d below. a. If a father has the defective x chromosome and the mother has good XX chromosomes, what is the probability that a son will inherit the disease? nothing (Type an integer or a decimal. Do not round.) b. If a father has the defective x chromosome and the mother has good XX chromosomes, what is the probability that a daughter will inherit the disease? nothing (Type an integer or a decimal. Do not round.) c. If a mother has one defective x…arrow_forwardA color-blind woman with Turner syndrome (XO) has a father who is color blind.Given that the gene for the color-blind condition is recessive and X-linked, provide a likely explanation for the origin of the color-blind and chromosome constitution in the color-blind woman. nondisjunction in the mother in meiosis I or II nondisjunction in the father at meiosis I no abnormalities had to occur to produce this daughter nondisjunction in the father in meiosis I or II nondisjunction in both the mother and father in meiosis I.arrow_forward
- From 2 to 6 percent of people with autism have an extra chromosome that consists of two long arms of chromosome 15. It includes two copies of the chromosome 15 centromere. Two normal copies of the chromosome are also present. What type of chromosome abnormality in a gamete can lead to this karyotype, which is called isodicentric 15?arrow_forwardA phenotypically normal woman has an abnormally structured chromosome 2, along with a normal homologue. She marries a phenotypically normal man with an abnormally structured chromosome 16 and a normal homologue. What is the probability of their child will have an abnormal chromosome 2 and 16? What is the probability that this child, having inherited both abnormal chromosomes, will now pass both abnormal chromosomes to its children?arrow_forwardA normal female is discovered with 45 chromosomes, one of which exhibits a Robertsonian translocation containing most of chromosomes 15 and 21. Discuss the possible outcomes in her offspring when her husband contains a normal karyotype.arrow_forward
- The autosomal (not X-linked) gene for brachydactyly, short fingers, is dominant to normal finger length. Assume that a female with brachydactyly in the heterozygous condition is married to a man with normal fingers. What is the probability that their first child will be a brachydactylous girl? ¼ 1/2 1/8 3/4 2/3arrow_forwardThe following Pedigree shows an unknown genetic disorder. The disorder is believed to be caused by single gene mutations. For the following disorder, determine whether the mutant gene is located on an autosome or X chromosome. arrow_forwardwhich genetic disorder matches below descriptions. extra 21st chromosome attaches to chromosome 14. Affected individual exhibit epichanthic folds of eyelids, simian crease in palms, and mental retardation. trisomy 18 Affected individuas have an elongated skull, hair lip, cleft palate, rocker-bottom feet. Life expectancy is about 10 weeks. trisomy 21. Affected indiviudals exhibit epicanthic folds of eyelids, protruding tongue, small, low set ears, and retardation.arrow_forward
- A normal mother has translocations on chromosomes 14:21. With respect to chromosomes 14:21, how many combinations of chromosomes are possible? How many gametes are viable? If the woman has children with an normal father, what is the probability that there is a daughter with Down Syndrome or a son with an unaffected phenotype?arrow_forwardAssuming no other abnormalities, classify each of the following human sex chromosome complements as to whether or not individuals with that complement will be morphologically male or female. Three human sex chromosome complements will be classified as male and three will be classified as female. XXY XYY XXX XO XY XXarrow_forwardAn individual heterozygous for a reciprocal translocation possesses the following chromosomes: A B • C D E F G A B • C D V W X R S • T U E F G R S • T U V W X Q. Draw the pairing arrangement of these chromosomes in prophase I of meiosis.arrow_forward
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