BIOLOGY:CONCEPTS+APPL.(LOOSELEAF)
10th Edition
ISBN: 9781305967359
Author: STARR
Publisher: CENGAGE L
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Textbook Question
Chapter 14, Problem 9SA
Alleles for Tay-Sachs disease are inherited in an autosomal recessive pattern. Why would two parents with a normal
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 c |
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Check out a sample textbook solutionStudents have asked these similar questions
Match 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…
If a genetic disease is inherited on the basis of an autosomal dominant gene, one would expect
to find which of the following?
A. Affected fathers have only affected children.
B. Affected mothers never have affected sons.
C. If both parents are affected, all of their offspring have the disease.
D. If a child has the disease, one of his or her grandparents also had the disease.
What is Mendelian inheritance?
a. Mendelian genes code an entire phenotype so that children will not be clones of their parents.
b. Mendelian genetics are those genes that code for dominant or recessive illnesses but only if no polygenic traits cancel them out.
c. Mendelian genes sit at one loci with one allele from Mom and one allele from Dad.
d. Mendelian genetics is when two or more genes at two or more loci express one trait
Chapter 14 Solutions
BIOLOGY:CONCEPTS+APPL.(LOOSELEAF)
Ch. 14 - Constructing a family pedigree is particularly...Ch. 14 - Prob. 2SACh. 14 - Prob. 3SACh. 14 - Prob. 4SACh. 14 - Prob. 5SACh. 14 - A trait that is present in a male child but not in...Ch. 14 - Color blindness is a case of ________ inheritance....Ch. 14 - Prob. 8SACh. 14 - Alleles for Tay-Sachs disease are inherited in an...Ch. 14 - Prob. 10SA
Ch. 14 - Prob. 11SACh. 14 - Prob. 12SACh. 14 - Prob. 13SACh. 14 - Klinefelter syndrome XXY can be easily diagnosed...Ch. 14 - Match the chromosome terms appropriately. ___...Ch. 14 - Does the phenotype indicated by the red circles...Ch. 14 - Human females have two X chromosomes XX; males...Ch. 14 - Somatic cells of individuals with Down syndrome...Ch. 14 - An allele responsible for Marfan syndrome Section...Ch. 14 - Both Duchenne muscular dystrophy and color...
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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
- A is a dominant gene for normal pigment, and a is its recessive allele for albinism (and pink eyes). B is a dominant gene for brown eyes, and b is its recessive allele (blue). What is the mother's genotype if two brown-eyed parents have fraternal twins, one with blue eyes and one with pink eyes (albino)? a. AaBb b. AaBB c. aaBb d. aabb e. AABBarrow_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_forwardWebbed 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 squarearrow_forward
- 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_forwardBoth of Ruth's parents have a round face, a dominant trait. Ruth, however, was born with a square face. What does Ruth's phenotype imply about her parents' genes? a. Ruth's parents are both heterozygous when it comes to their facial shape. b. When it comes to facial shape, Ruth's parents gave her one dominant gene and one recessive gene. c. Ruth's parents are both homozygous when it comes to their facial shape. d. Ruth's sister also has a square face.arrow_forwardTwo albino parents have four unaffected children. If albinism in the parents is given by mutations on two different genes (A and B) and complementation is observed in all four children, what are the genotypes of the parents? A. AaBb and AABB B. AABb and AaBB C. both parents are AaBb D. AAbb and BBaaarrow_forward
- Please choose the correct answer. If a recessive mutation kills an individual during the early stages of its development, what is the possible mode of inheritance exhibited if a recessive F1 with heterozygous parents survives? a. epigenetic inheritance b. maternal inheritance c. maternal effect d. organelle inheritancearrow_forwardPolydactyly 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_forwardIf a genetic disease is inherited as an autosomal recessive, one would expect to find which of the following? A. Two affected individuals never have an unaffected child. B. Two affected individuals have affected male offspring but no affected female children. C. If a child has the disease, one of his or her grandparents will have had it. D. In a marriage between an affected individual and an unaffected one, all the children are unaffected.arrow_forward
- The condition phenylketonuria is caused by a recessive allele. There are two carriers who have progeny.a. Give the gene notation. b. Give the expected genotypic and phenotypic ratios. c. What is the probability that their child will be heterozygous if they have a normal child?d. What is the probability of having two affected children and one normal child if they have three children?arrow_forwardDuchenne muscular dystrophy is sex linked and usually affects only males. Victims of the disease become progressively weaker, starting early in life.a. What is the probability that a woman whose brother has Duchenne’s disease will have an affected child?b. If your mother’s brother (your uncle) had Duchenne’s disease, what is the probability that you have received the allele?c. If your father’s brother had the disease, what is the probability that you have received the allele?arrow_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
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