INTRO TO GEN ANALYSIS W/ACHIEVE ACCESS
12th Edition
ISBN: 9781319423865
Author: Griffiths
Publisher: MAC HIGHER
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Chapter 2, Problem 55P
a.
Summary Introduction
To determine: The probability of taste detecting trait in the progeny.
Introduction: The human consists of 23 pairs of chromosomes, condensed form of chromatids which divide during cell division into daughter cells. The human has 22 autosomes and one pair of sex chromosomes. The sex chromosomes determine the sex in an individual based on the type of sex chromosomes that are present in the fusing gametes.
b.
Summary Introduction
To determine: The probability that the first two children will be taster.
Introduction: When the two or more alleles equally expressed themselves through the
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a. The ability to taste the chemical phenylthiocarbamideis an autosomal dominant phenotype, and the inabilityto taste it is recessive. If a taster woman with a nontasterfather marries a taster man who in a previous marriagehad a nontaster daughter, what is the probability thattheir first child will be(1) A nontaster girl(2) A taster girl(3) A taster boyb. What is the probability that their first two childrenwill be tasters of either sex?
Part VI: Discussion
1. Write the genetic designation for:
a. a male
b. a female
2. Which parent determines the sex of the offspring in humans? Explain.
3. Explain the term "autosomal."
4. In humans, right-handed is dominant to left. Free earlobes are dominant to attached. These are
autosomal characteristics. A right-handed man with attached earlobes whose mother was lefthanded
marries a left-handed woman with free earlobes whose mother had attached earlobes. You are the
genetic counselor. Construct a Punnett square to determine the types of children this couple could
produce.
A. Color-blindness is a recessive, sex-linked disorder in humans. A color-
blind man has a child with a woman who is a carrier of the disorder.
KEY: X= normal vision XC = color-blindness
2. Illustrate using a Punnett square the probability of having children
who will have normal vision and children who will be color-blind.
Guide Questions:
a. What is the genotype of the male?.
b. What is the genotype of the female?
c. What is the chance that the child will be color-blind?
d. What is the chance that a daughter will be color-blind?
e. What is the chance that a son will be color-blind?
Chapter 2 Solutions
INTRO TO GEN ANALYSIS W/ACHIEVE ACCESS
Ch. 2 - Prob. 1PCh. 2 - Prob. 2PCh. 2 - Prob. 3PCh. 2 - Prob. 4PCh. 2 - Prob. 5PCh. 2 - Prob. 6PCh. 2 - Prob. 7PCh. 2 - Prob. 8PCh. 2 - Prob. 9PCh. 2 - Prob. 10P
Ch. 2 - Prob. 11PCh. 2 - Prob. 12PCh. 2 - Prob. 13PCh. 2 - Prob. 14PCh. 2 - Prob. 15PCh. 2 - Prob. 17PCh. 2 - Prob. 18PCh. 2 - Prob. 19PCh. 2 - Prob. 20PCh. 2 - Prob. 21PCh. 2 - Prob. 22PCh. 2 - Prob. 23PCh. 2 - Prob. 24PCh. 2 - Prob. 25PCh. 2 - Prob. 26PCh. 2 - Prob. 27PCh. 2 - Prob. 28PCh. 2 - Prob. 29PCh. 2 - Prob. 30PCh. 2 - Prob. 31PCh. 2 - Prob. 32PCh. 2 - Prob. 33PCh. 2 - Prob. 34PCh. 2 - Prob. 35PCh. 2 - Prob. 36PCh. 2 - Prob. 37PCh. 2 - Prob. 38PCh. 2 - Prob. 39PCh. 2 - Prob. 40PCh. 2 - Prob. 41PCh. 2 - Prob. 42PCh. 2 - Prob. 43PCh. 2 - Prob. 44PCh. 2 - Prob. 45PCh. 2 - Prob. 46PCh. 2 - Prob. 47PCh. 2 - Prob. 48PCh. 2 - Prob. 49PCh. 2 - Prob. 50PCh. 2 - Prob. 51PCh. 2 - Prob. 52PCh. 2 - Prob. 53PCh. 2 - Prob. 54PCh. 2 - Prob. 55PCh. 2 - Prob. 56PCh. 2 - Prob. 56.1PCh. 2 - Prob. 56.2PCh. 2 - Prob. 56.3PCh. 2 - Prob. 56.4PCh. 2 - Prob. 56.5PCh. 2 - Prob. 56.6PCh. 2 - Prob. 56.7PCh. 2 - Prob. 56.8PCh. 2 - Prob. 56.9PCh. 2 - Prob. 56.10PCh. 2 - Prob. 56.11PCh. 2 - Prob. 56.12PCh. 2 - Prob. 56.13PCh. 2 - Prob. 56.14PCh. 2 - Prob. 56.15PCh. 2 - Prob. 57PCh. 2 - Prob. 58PCh. 2 - Prob. 59PCh. 2 - Prob. 60PCh. 2 - Prob. 61PCh. 2 - Prob. 62PCh. 2 - Prob. 63PCh. 2 - Prob. 64PCh. 2 - Prob. 65PCh. 2 - Prob. 67PCh. 2 - Prob. 68PCh. 2 - Prob. 69PCh. 2 - Prob. 70PCh. 2 - Prob. 71PCh. 2 - Prob. 72PCh. 2 - Prob. 73PCh. 2 - Prob. 74PCh. 2 - Prob. 75PCh. 2 - Prob. 76PCh. 2 - Prob. 77PCh. 2 - Prob. 78PCh. 2 - Prob. 79PCh. 2 - Prob. 80PCh. 2 - Prob. 81PCh. 2 - Prob. 82PCh. 2 - Prob. 83PCh. 2 - Prob. 84PCh. 2 - Prob. 85PCh. 2 - Prob. 86PCh. 2 - Prob. 87PCh. 2 - Prob. 88PCh. 2 - Prob. 89PCh. 2 - Prob. 90PCh. 2 - Prob. 91PCh. 2 - Prob. 1GSCh. 2 - Prob. 2GSCh. 2 - Prob. 3GS
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- A Father and Mother are both carriers of the autosomal recessive condition known as albinism. They have one child, and a second child two years later. Their first child was not albino. Knowing this, you can say that the probability of the second child having albinism is Note Albinism is the result of a lack of pigmentation in skin and other cells. O a. 100% b. dependent on the the genotype of the first child O C. 50% O d. 25%arrow_forward12. A. B. C. A certain type of migraine headache (M) is dominant to no migraines (m). What is the genotype of a man who has migraine headaches if his father did not have them? What is the genotype of a man who has migraine headaches if his mother did not have them? If a woman without migraines marries a man who is heterozygous for migraines, what would you expect for the genotypes and phenotypes of their children? If two people who are heterozygous for migraines marry and have children, what would you expect for the genotypes and phenotypes of the children.arrow_forwardre ||| E 6. Label the genotypes for this pedigree of an X-linked recessive disorder (red- green colorblindness). (a) 2 2 3 1 3 a. How do you know? b. Label the genotypes. 4 O To 2 4 5 5 6 6 7. Is the following pedigree autosomal recessive, autosomal dominant or X-linked recessive? 2 8 O T 58arrow_forward
- 1. An albino man whose parents are both normal marries a woman one of whose parents is normal and the other albino. She has an albino sister. The couple has a normal son. a. Is albinism a dominant or a recessive trait? Explain your answer. b. Give the genotypes of all the persons involved. c.The couple plans to have more kids. What is the probability of their second child being normal?arrow_forwardFor Modes of Inheritance for Single Gene Traits choose between • Autosomal Dominant • Autosomal Recessive • X-linked Dominant • X-linked Recessive • Y-linked • Mitochondrial Let us assume that alleles for these traits follow complete dominance.arrow_forward1. Mary and Joe are both healthy individuals. Joe has a mother who suffered from cystic fibrosis, an autosomal recessive disorder. Mary has been genetically tested in order to find out if she has the allele responsible for this disease and her tests came out positive. They are planning on having two children together in the near future. What is the probability that she and Joe will have either 2 boys who have the disorder, OR that they have one boy who has the disorder and one boy who does not? (in other words, what is the probability that any of these two outcomes takes place? a) 1/8 b) 1/16 c) 3/32 d) 1/64 e) 9/64arrow_forward
- . Assuming no involvement of the Bombay phenotype(in case you’ve already read ahead to Section 3.2):a. If a girl has blood type O, what could be the genotypes and corresponding phenotypes of her parents?b. If a girl has blood type B and her mother has bloodtype A, what genotype(s) and correspondingphenotype(s) could the other parent have?c. If a girl has blood type AB and her mother is alsoAB, what are the genotype(s) and correspondingphenotype(s) of any male who could not be thegirl’s father?arrow_forwardPlease 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_forward1. Autosomes B.Sex chromosomes C.Chromosome DDominant Recessive Practice: Heredity Vocabulary Match the following terms in the box with the appropriate definition. Homozygous G.Heterozygous H.Phenotype Genotype ✓ Law of Dominance When several genes influence a trait. 2. ✓ A version of a gene 3. K-Law of Segregation Law of Ind. Assortment Incomplete dominance Codominance Polygenic Inheritance Multiple Alleles Q. Sex-Linked BLinked genes S. Epistasis Karyotype Carrier Allele W. Protein X DNA Gene When the heterozygous genotype results in a phenotype where both alleles are fully and separately expressed 4. प्रे Chromosomes 1-44 in a human 5. N Only expressed in the homozygous state 6. ✓ Genes that travel on the X chromosome 7. ✓ Chromosomes line up randomly during metaphase therefore it is possible for any combination of chromosomes to be passed on from parent to offspring. 8. T 9. A diagram that shows homologous chromosome pairs C The macromolecule that runs your body and expresses your…arrow_forward
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