Biology: Life on Earth with Physiology Plus Mastering Biology with Pearson eText -- Access Card Package (11th Edition)
11th Edition
ISBN: 9780133910605
Author: Gerald Audesirk, Teresa Audesirk, Bruce E. Byers
Publisher: PEARSON
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Chapter 11.3, Problem 1CYL
- describe the pattern of inheritance of a trait controlled by a single gene with two alleles, one dominant and one recessive?
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Determine the mode of inheritance:
Homozygous recessive die from fatal disorder, when a specific enzyme activity is absent. Heterozygous exhibit wild type phenotype but have intermediate level of gene expression resulting in 1/2 of the wild type enzyme activity when compared to Homozygous normal non-carriers. Based on the levels of gene expression ALONE, the mode of inheritance is?‐---------------
In genetics, what does a genotype of Hh signify?
Choose 1 answer:
Choose 1 answer:
(Choice A)
A
Homozygous; two dominant alleles
(Choice B)
B
Homozygous; two recessive alleles
(Choice C)
C
Heterozygous; one dominant allele and one recessive allele
(Choice D)
D
Homozygous; one dominant allele and one recessive allele
In sex-linked inheritance, if a colour blind man
mates with a heterozygous woman, what is the
expected ratio of phenotypes among the offsprings?
normal female : heterozygous female : normal
male : colour-blind male (1 : 1 :1: 1)
normal female : normal male : colour-blind
male (2 :1: 1)
normal female : heterozygous female : normal
male (1:1:2)
heterozygous female: colour blind female:
normal male: colour-blind male (1: 1: 1: 1)
Chapter 11 Solutions
Biology: Life on Earth with Physiology Plus Mastering Biology with Pearson eText -- Access Card Package (11th Edition)
Ch. 11.1 - describe the relationships among chromosomes, DNA,...Ch. 11.1 - Prob. 2CYLCh. 11.2 - distinguish between self-fertilization and...Ch. 11.2 - Prob. 2CYLCh. 11.3 - Sudden Death on the court Many traits, in humans...Ch. 11.3 - describe the pattern of inheritance of a trait...Ch. 11.3 - Prob. 1TCCh. 11.3 - Prob. 2CYLCh. 11.3 - Prob. 3CYLCh. 11.4 - Prob. 1CYL
Ch. 11.4 - Prob. 1TCCh. 11.4 - Prob. 2CYLCh. 11.4 - Prob. 2TCCh. 11.4 - Prob. 3CYLCh. 11.5 - Prob. 1CSCCh. 11.5 - Prob. 1CYLCh. 11.5 - Prob. 1HYEWCh. 11.5 - Prob. 1TCCh. 11.5 - explain how polygenic inheritance and...Ch. 11.6 - describe how the patterns of inheritance differ...Ch. 11.7 - Prob. 1CYLCh. 11.7 - explain why most sex-linked traits are controlled...Ch. 11.7 - describe the pattern of inheritance of sex-linked...Ch. 11.8 - Prob. 1CSRCh. 11.8 - use pedigrees to determine the pattern of...Ch. 11.8 - Prob. 1ETCh. 11.8 - Prob. 1TCCh. 11.8 - Prob. 2CYLCh. 11.8 - Prob. 2ETCh. 11 - Prob. 1ACCh. 11 - An organism is described as Rr, with red coloring....Ch. 11 - In certain cattle, hair color can be red...Ch. 11 - Prob. 1MCCh. 11 - Define the following terms: gene, allele,...Ch. 11 - Prob. 2ACCh. 11 - Prob. 2FIBCh. 11 - Prob. 2GPCh. 11 - Prob. 2MCCh. 11 - Prob. 2RQCh. 11 - Prob. 3FIBCh. 11 - Prob. 3GPCh. 11 - Prob. 3MCCh. 11 - Prob. 3RQCh. 11 - Genes that are present on one sex chromosome but...Ch. 11 - Prob. 4GPCh. 11 - Prob. 4MCCh. 11 - Prob. 4RQCh. 11 - Prob. 5FIBCh. 11 - Prob. 5GPCh. 11 - Prob. 5MCCh. 11 - Prob. 5RQCh. 11 - Prob. 6GPCh. 11 - Prob. 6RQCh. 11 - In the couple described in Problem 6, the woman...
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- For a recessive condition, two normal heterozygous individuals have children. What is the likelihood of their children being affected by this condition? What is the likelihood of their children being carriers without the condition? What is the likelihood of their asymptomatic children being carriers? Suppose that an individual with the condition has children with a heterozygous individual, what is the likelihood of their children being carriers?arrow_forwardWhich of the following defines polygenic inheritance? An inheritance pattern in which one allele is not fully dominant over another, so the heterozygous phenotype is an intermediate blend of the two homozygous phenotypes An inheritance pattern in which the full and separate phenotypic effects of two alleles are apparent in heterozygous individuals An inheritance pattern in which a single gene affects multiple traits A pattern of inheritance in which multiple genes affect one traitarrow_forwardYou possess two alleles for each of your genes. (One from the paternal side and one from the maternal side in each homologous pair of chromosomes.) In simple inheritance, having at least one dominant allele (form of the gene) means you will display the dominant phenotype, and the only way to display the recessive phenotype is to have two recessive alleles. For example, individuals with the genotypes RR and Rr can roll their tongue (into a U shape). If you cannot roll your tongue, then you know with certaintly you have the genotype rr. If you can roll your, you would write your genotype as R- (R followed by a dash since you might not know if you are RR or Rr, but either way, you display the dominant phenotype because the first letter is capital.) Match the following traits with their proper genotype using the letters provided in the lab handout. left arm on top when crossing arms blue eyes no middigital hair widow's peakarrow_forward
- Color-blindness (c) is a sex-linked recessive trait, while normal color vision (C) is dominant: If two normal-visioned parents have a color-blind son, what are the parent's genotypes? ~What are the chances that their children will be color-blind?arrow_forwardExplain the Multiple-Gene Hypothesis for Quantitative Inheritance ?arrow_forwardIf traits are inherited together, for example if Mendel found that this pea plant always had yellow and round seeds or green and wrinkled but never yellow and wrinkled or green and round. The explanation for this must be that; a) There is one gene controlling both phenotypes Ob) The genes are located close together on the same chromosome c) The genes are located on the same chromosome d) The genes are located close together on the same chromosome or there could be one gene controlling both phenotypesarrow_forward
- Describe the differences between an incompletely dominant trait and a codominant trait.arrow_forwardPls answer the very last question. “ suppose that lll-2 and lll-5 were to have a child. What is the probability that their first child will be have the disorder?”arrow_forwardIf an individual is heterozygous for a gene with two alleles, one dominant and one recessive, what would the phenotype be?arrow_forward
- Explain the concept of mendal's law of inheritence?arrow_forwardExplain the term maternal inheritance? Which characters show this type of inheritance?arrow_forwardIn humans, cystic fibrosis and albinism are both inherited as independently assorting autosomal recessive traits. Use f to represent the recessive allele for cystic fibrosis and F for the allele for the unaffected condition. Use A to represent the dominant allele for normal melanin and a for the recessive allele for albinism. A man is albino and heterozygous for cystic fibrosis. His wife has the unaffected phenotype for both traits, although her father had cystic fibrosis and her mother is albino. 4a. What is the genotype of the wife 4b.What is the probability that a child of this couple is albino and has cystic fibrosis? 4c.What is the probability that a child of this couple is a girl who is albino and has cystic fibrosis? 4d.What is the probability that a child of this couple is normal for both traits?arrow_forward
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