SEELEY'S ANATOMY+PHYSIOLOGY
12th Edition
ISBN: 9781260172195
Author: VanPutte
Publisher: RENT MCG
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Chapter 29, Problem 24RAC
Summary Introduction
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F1 and F2 offspring with given genders and disease phenotypes.
The data are generated from an initial parental cross.
One parent displays the disease phenotype and one displays the wild-type (WT) phenotype.
The WT parent always has a homozygous genotype.
There are three possible modes of inheritance that underlie
the generation of the data. All are monogenic. They are:
(i) Autosomal Recessive.
(ii) Homozygous Lethal Dominant.
(iii) Autosomal Dominant.
One's phenotype is determined by their genotype at the disease locus
and the mode of inheritance, as we have seen with Punnett Square.
on the F2 data and make a decision, based on your statistical analysis, as to whether
you reject or do not reject the computer-generated model of inheritance as being consistent
with the observed data.
The mode of inheritance you are to test on the observed data is autosomal recessive.
PARENTAL CROSS
Parental cross: Father with disease phenotype, Mother with wild-type phenotype.
F1 DATA
Phenotype…
A couple are both phenotypically normal but their son suffers from hemophilla, a sex linked recessive disorder. What fraction of their children are likely to suffer from hemophilia. what fraction are likely to be carriers.
Humans homozygous for the sickle cell allele have sickle cell anemia. A human that is heterozygous for the sickle cell allele is generally protected from both sickle cell anemia and malaria. This is an example of
incomplete penetrance.
overdominance.
multiple allele systems.
polygenic inheritance.
codominance
Chapter 29 Solutions
SEELEY'S ANATOMY+PHYSIOLOGY
Ch. 29.1 - Describe the three parts of the prenatal period,...Ch. 29.1 - Distinguish between clinical age and postovulatory...Ch. 29.1 - Prob. 3AYPCh. 29.1 - Prob. 4AYPCh. 29.1 - Prob. 5AYPCh. 29.1 - What events occur during the first week after...Ch. 29.1 - Prob. 7AYPCh. 29.1 - Explain the process of implantation and the...Ch. 29.1 - Prob. 9AYPCh. 29.1 - Prob. 10AYP
Ch. 29.1 - Prob. 11AYPCh. 29.1 - Prob. 12AYPCh. 29.1 - Prob. 13AYPCh. 29.1 - Prob. 14AYPCh. 29.1 - Describe the process involved in forming the face....Ch. 29.1 - Describe the formation of the following major...Ch. 29.1 - Explain the formation of the following endocrine...Ch. 29.1 - Prob. 18AYPCh. 29.1 - Prob. 19AYPCh. 29.1 - Prob. 20AYPCh. 29.1 - Prob. 21AYPCh. 29.1 - Prob. 22AYPCh. 29.2 - Prob. 23AYPCh. 29.2 - Describe the hormonal changes that take place...Ch. 29.3 - What changes occur in the newborn's cardiovascular...Ch. 29.3 - Prob. 26AYPCh. 29.3 - What does the score measure?Ch. 29.3 - What are congenital disorders? What are some...Ch. 29.3 - Prob. 29AYPCh. 29.4 - Which hormones ore involved in preparing the...Ch. 29.4 - Describe the events of milk production and milk...Ch. 29.4 - Prob. 32AYPCh. 29.5 - Prob. 33AYPCh. 29.6 - Prob. 34AYPCh. 29.6 - Prob. 35AYPCh. 29.6 - Prob. 36AYPCh. 29.6 - Prob. 37AYPCh. 29.6 - Prob. 38AYPCh. 29.6 - What role does genetics play in aging?Ch. 29.6 - Prob. 40AYPCh. 29.7 - What is genetics?Ch. 29.7 - Prob. 42AYPCh. 29.7 - What are alleles? If tall (T) plants are dominant...Ch. 29.7 - Prob. 44AYPCh. 29.7 - What are the number and type of chromosomes in the...Ch. 29.7 - Prob. 46AYPCh. 29.7 - Prob. 47AYPCh. 29.7 - Distinguish among complete om nonce, Incomplete...Ch. 29.7 - Prob. 49AYPCh. 29.7 - How are sex-linked traits inherited? Give on...Ch. 29.7 - What is meiosis? How does it differ from mitosis?...Ch. 29.7 - Prob. 52AYPCh. 29.7 - Prob. 53AYPCh. 29.7 - What causes the genetic disorder Down syndrome?Ch. 29 - Prob. 1RACCh. 29 - Given these structure: (1) blastocyst (2) morula...Ch. 29 - Prob. 3RACCh. 29 - Prob. 4RACCh. 29 - Prob. 5RACCh. 29 - Prob. 6RACCh. 29 - Prob. 7RACCh. 29 - Prob. 8RACCh. 29 - Prob. 9RACCh. 29 - Prob. 10RACCh. 29 - Prob. 11RACCh. 29 - Prob. 12RACCh. 29 - Prob. 13RACCh. 29 - Prob. 14RACCh. 29 - Which hormones cause differentiation of sex organs...Ch. 29 - Prob. 16RACCh. 29 - Prob. 17RACCh. 29 - Prob. 18RACCh. 29 - Prob. 19RACCh. 29 - Prob. 20RACCh. 29 - Prob. 21RACCh. 29 - Which of these terms is correctly matched with its...Ch. 29 - Prob. 23RACCh. 29 - Prob. 24RACCh. 29 - Prob. 25RACCh. 29 - Prob. 1CTCh. 29 - A physician tells a woman that she is pregnant and...Ch. 29 - Prob. 3CTCh. 29 - Prob. 4CTCh. 29 - Prob. 5CTCh. 29 - Prob. 6CTCh. 29 - Prob. 7CTCh. 29 - Prob. 8CTCh. 29 - Prob. 9CTCh. 29 - Prob. 10CT
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- Recessives Allele, an allele that is fully expressed in the phenotype of a heterozygote. Select one: True Falsearrow_forwardHemophilia is a sex-linked trait. A person with hemophilia is lacking certain proteins that are necessary for normal blood clotting. Hemophilia is caused by a recessive allele so use "N" for normal and "n" for hemophilia. Since hemophilia is sex-linked, remember a woman will have two alleles (NN or Nn or nn) but a man will have only one allele (N or n). A woman who is heterozygous (a carrier) for hemophilia marries a normal man: a.What are the genotypes of the parents? b.What is the probability that a male offspring will have hemophilia? c. What is the probability of having a hemophiliac female offspring?arrow_forwardTrue or false? Codominance and complete dominance establish the same pattern of inheritance.arrow_forward
- What is the most likely mode of inheritance of the trait shown in the pedigree? - Y-linked - X-linked recessive - autosomal recessive - autosomal dominant - X-linked dominantarrow_forwardHemophilia is inherited as a sex-linked recessive trait. A non-hemophilic man marries a non-hemophilic woman whose father had hemophilia. With respect to this information, indicate all possible genotypes their children could possibly have. Show ALL work using punnett squares.arrow_forwardIf a trait is X-linked, which of the following statements is true? Two recessive alleles are needed to express that trait. A female with one recessive allele will express that trait. A female can be a carrier, affected or unaffected. The trait is inherited from father to son. The gene is carried on the Y chromosome.arrow_forward
- 모오모오 What is the most likely mode of transmission of the trait? autosomal dominant sex-linked recessive sex-linked dominant autosomal recessivearrow_forwardForms and Expressions of Alleles Classify each of the following phenotypes and genotypes using the vocabulary from this lesson. Phenotype Brown eyes/ Genotype one dominant brown allele and one Phenotype Blue eyes/Genotype two Phenotype Brown eyes/Genotype two recessive blue alleles dominant brown alleles recessive blue allele :: ::: ::: homozygous recessive homozygous dominant heterozygous Save Submit Google Chrome edu DELL 4 7 8. 9. tw #arrow_forwardIn humans, hemophilia is a sex-linked trait. Females can be normal, carriers, or have the disease. Males will either have the disease or not (but they won’t ever be carriers). X H X H = female, non-hemophilic X H X h = female, carrier X h X h = female, hemophilia X H Y = male, non-hemophilic X h Y= male, hemophiliac a.) Show the cross of a man who has hemophilia with a woman who is a carrier. What is the probability that their children will have the disease? b.) A woman who is a carrier marries a non-hemophilic man. Show the cross. What is the probability that their children will have hemophilia? What sex will a child in the family with hemophilia be? c.) A woman who has hemophilia marries a non-hemophilic man. How many of their children will have hemophilia, and what is their sex?arrow_forward
- Hemophilia is a blood disorder which is sex-linked. A woman carrier has children with a normal man. Determine the chances for girls and boys with hemophilia. [Remember that females have the XX genotype and males have the XY genotype. Do not place an allele on the Y chromosome. Example: XN Xn for female; Xn Y for male]arrow_forwardThere is a practical joker in the maternity ward who removed all the baby ID bracelets. There are two babies that cannot be easily distinguished, and the parents want to be sure they get the right ones back, so the doctors do a blood test. Parents 1: mom is heterozygous type A and the dad is type O. Blood Type (phenotypel Posible Genotype(s) AA of AD A 88 o B0 Parents 2: mom is heterozygous type A and dad has AB. AS AB 00 Babies: baby 1 has blood type AB and baby 2 has blood type O. Determine what baby goes with which parents. Explain how you know. Provide evidence and reasoning by explaining multiple alleles inheritance and your Punnett squares results. Be sure to include: Claim: Answer the question: Which baby goes with parent 1 Which baby goes with parent 2arrow_forwardConsidering a common autosomal recessive trait: (Read each statement carefully. Select all of the statements below that are true (that you agree with). Leave any statements that are false (that you do not agree with) un- selected.) the unaffected biological siblings of an affected person should be heterozygotes. an unaffected woman and an affected man have at most a 100% probability of having a affected child. an affected person should have an affected parent. The unaffected offspring of an affected parent must be carriers.arrow_forward
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