BIOLOGY
12th Edition
ISBN: 9781260169614
Author: Raven
Publisher: RENT MCG
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Textbook Question
Chapter 13, Problem 1U
Why is the white-eye
a. Because the trait is dominant
b. Because the trait is recessive
c. Because the allele is located on the X chromosome and males only have one X
d. Because the allele is located on the Y chromosome and only males have Y chromosomes
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Students have asked these similar questions
Which statement about the pattern of inheritance for a recessive X-linked allele is true?
A. Unaffected parents can produce daughters who are affected.
B. Unaffected parents can have sons who are affected and daughters who are carriers.
C. Unaffected fathers can be carriers.
D. Affected parents do not produce affected children.
E. Every affected person has an affected parent.
Organism X has the genotype Ccdd. How many different types of gametes
can it make and in what proportion? *
A. 3 Cd 1 cd
B. 1 CD: 1 Cd : 1 cD 1 cd
C. 1 Cc : 1 dd
D. 1 Cd 1 cd
A human female "carrier" who is heterozygous for the recessive, sex-linked
trait hemophilia (XHXH), marries a normal male (XHY). What proportion of
their male progeny will show the trait?
A. 1/4
B. 1/2
C. 0
D. All
In humans, potential or expecting parents can be tested for the presence of the allele for the autosomal recessive cystic fibrosis. Which combination of parents are LEAST likely to produce a child with cystic fibrosis?
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2 parents with cystic fibrosis
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2 parents without cystic fibrosis
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1 parent without cystic fibrosis and 1 with cystic fibrosis
D.
2 parents who do not know if they have cystic fibrosis
Chapter 13 Solutions
BIOLOGY
Ch. 13.1 - Describe sex-linked inheritance in fruit flies.Ch. 13.1 - Prob. 2LOCh. 13.2 - Prob. 1LOCh. 13.2 - Explain the genetic consequences of dosage...Ch. 13.3 - Prob. 1LOCh. 13.4 - Prob. 1LOCh. 13.4 - Explain the relationship between frequency of...Ch. 13.4 - Prob. 3LOCh. 13.5 - Prob. 1LOCh. 13.5 - Prob. 2LO
Ch. 13.5 - Prob. 3LOCh. 13 - Inquiry question Mendel did not examine plant...Ch. 13 - What would Mendel have observed in a dihybrid...Ch. 13 - Prob. 2DACh. 13 - Why is the white-eye phenotype always observed in...Ch. 13 - In an organisms genome, autosomes are a. the...Ch. 13 - What cellular process is responsible for genetic...Ch. 13 - The map distance between two genes is determined...Ch. 13 - How many map units separate two alleles if the...Ch. 13 - How does maternal inheritance of mitochondrial...Ch. 13 - Which of the following genotypes due to...Ch. 13 - Prob. 1ACh. 13 - As real genetic distance increases, the distance...Ch. 13 - Down syndrome is the result of trisomy for...Ch. 13 - Genes that are on the same chromosome can show...Ch. 13 - The A and B genes are 10 cM apart on a chromosome....Ch. 13 - Prob. 6ACh. 13 - Color blindness is caused by a sex-linked,...Ch. 13 - Assume that the genes for seed color and seed...Ch. 13 - A low frequency of calico cats are male (about...
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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
- Phenylketonuria (PKU) is a disease that results from a recessive gene.Suppose that two unaffected parents produce a child with PKU. a. What is the probability that a sperm from the father will contain the PKU allele?b. What is the probability that an egg from the mother will contain the PKU allele?c. What is the probability that their next child will have PKU?d. What is the probability that their next child will be heterozygous for the PKU gene?arrow_forwardPhenylketonuria (PKU) is a disease that results from a recessive gene. Suppose that two unaffected parents produce a child with PKU. a. What is the probability that a sperm from the father will contain the PKU allele? b. What is the probability that an egg from the mother will contain the PKU allele? c. What is the probability that their next child will have PKU? d. What is the probability that their next child will be heterozygous for the PKU gene?arrow_forwardWhich observation led Thomas Morgan to realize that the gene for fruit fly eye color was located on a sex chromosome? a. He noticed that only male F2 flies could have white eyes; no females displayed this trait. b. He saw that the F2 generation of flies had the classic 3:1 phenotypic ratio of red eyes to white eyes c. He read it in a biology textbook d. He noticed that only mutant flies had white eyesarrow_forward
- If a male is homozygous dominant for a trait, that parent’s genotype might be DD. If the female is heterozygous for the same trait, her type would be Dd. a. How many genetically different sperm can the male produce? b. Using punnet square, determine the expected genotypic ratios of their offspring. c. What are the expected phenotypic ratios?arrow_forwardMatch the pattern of inheritance to the appropriate term. A. Heterozygotes with different alleles of the DTL1 gene survive better than homozygotes B. The disease is usually passed from a mother to all children C. Pure-breeding pumpkin plants grown on sandy soil have bigger seeds than plants of the same pure-breeding lineage grown on peaty soil. D. A cross between a true-breeding plant with serrated leaf edges and a true- breeding plant with smooth leaf edges produces an F1 generation with 88% plants with serrated leaves. E. A cross between two heterozygotes, DdFf, produces offspring in three phenotypic groups; Long wings in offspring with genotype D_F_, short wings in offspring with D_ff, and no wings in offspring with the genotypes ddF_ and ddff. F. Individuals homozygous for a mutation in SME have a heightened sense of smell and large earlobes. G. Grey chickens bred together have offspring that are black, grey and white in a 1:2:1 ratio H.Alleles at locus S…arrow_forwardDefine epistasis? a. Allelic variation at two different genes adds together in order to produce a phenotypic outcome b. Genetic variation and environmental variation both affect a given phenotype c. Allelic variation at one gene prevents or conceals the phenotypic consequences of allelic variation at a different gene d. Allelic variation at single gene affects many different phenotypes e. Genes that are near the start of a gene cluster are expressed before genes near the end of the clusterarrow_forward
- On occasion, a trait that appears to be autosomal is produced in unexpected ratios in male and female offspring. What is this an example of? A. codominance B. sex-linked genes C. multiple alleles D. amniocentesisarrow_forwardHow is this trait inherited? A. The trait is epistatic. B. The trait is X-linked. C. The trait is dominant. D. The trait is recessive.arrow_forwardBaldness is a phenomenon where individuals lose hair as they grow older. As an X-linked recessive gene, what instances do females manifest this trait? a. heterozygous recessive b. heterozygous dominant c. homozygous recessive d. homozygous dominantarrow_forward
- Polydactyly is a congenital physical anomaly in in humans, dogs, cats; and having supernumerary fingers or toes. If it is an autosomal dominant trait, when is a genotype of a person that shows normal phenotype? a. heterozygous recessive b. heterozygous dominant c. homozygous recessive d. homozygous dominantarrow_forwardIn humans, the allele for colorblindness is found on the X chromosome and is recessive. If a woman is colorblind and her partner is not colorblind, what percent of their sons and/or daughters will be colorblind? A. 50% sons colorblind , 100% Daughters colorblind B. 0% sons colorblind , 100% Daughters colorblind C. 50% sons colorblind , 50% Daughters colorblind D. 100% sons colorblind, 0% Daughters colorblindarrow_forwardHemophilia is a disease caused by a gene found on the X chromosome. Therefore, it is a sex-linked disease which is caused by the recessive allele. Suppose, a man with hemophilia marries a woman who is homozygous dominant for the trait. Predict the genotype of the man. (XH = normal; Xh= hemophiliac) * a. XH Y b. XHXh c. XhXh d. Xh Yarrow_forward
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