QUESTION 13Use the pedigrees below to answer the corresponding. What is the most likely mode of inheritance for this trait?11a. MitochondrialOb. Autosomal dominantOc. X-linked recessiveOd. Autosomal recessiveOe. Y-linked

Name: QUESTION 13Use the pedigrees below to answer the corresponding. What
Uploaded: 2024-03-20T06:43:04.000Z
Channel: Bartleby
Description: QUESTION 13Use the pedigrees below to answer the corresponding. What is the most likely mode of inheritance for this trait?11a. MitochondrialOb. Autosomal dominantOc. X-linked recessiveOd. Autosomal recessiveOe. Y-linked

Introduction : A chart which displays the affected members of a family by genetic diseases in the…

Science

Biology

Use the pedigrees below to answer the corresponding. What is the most likely mode of inheritance for this trait? 11 E a. Mitochondrial Ob. Autosomal dominant Oc. X-linked recessive Od. Autosomal recessive e. Y-linked

Use the pedigrees below to answer the corresponding. What is the most likely mode of inheritance for this trait? 11 E a. Mitochondrial Ob. Autosomal dominant Oc. X-linked recessive Od. Autosomal recessive e. Y-linked

Human Heredity: Principles and Issues (MindTap Course List)

11th Edition

ISBN:9781305251052

Author:Michael Cummings

Publisher:Michael Cummings

Chapter4: Pedigree Analysis In Human Genetics

Section: Chapter Questions

Problem 20QP: Analysis of X-Linked Dominant and Recessive Traits The following is a pedigree for a common genetic...

See similar textbooks

Similar questions

QUESTION 10 Consider the following pedigree. With no other information provided, what is the most likely mode of transmission (or mode of inheritance) of the allele for the unusual trait? autosomal dominant sex-linked recessive autosomal recessive O sex-linked dominant
QUESTION 4 Look at the pedigree below. Which mode(s) of inheritance could explain this? Select all that apply. OY-linked O X-linked recessive O autosomal recessive O x-linked dominant O autosomal dominant O mitochondrial
QUESTION 22 Consider whether the mode of inheritance for each of the pedigrees below is autosomal dominant or autosomal recessive Pedigree I Both pedigrees show autosomal dominant modes of inheritance Pedigree I is autosomal dominant while pedigree II is autosomal recessive O Pedigree I is autosomal recessive while pedigree II is autosomal dominant O Both pedigrees show autosomal recessive modes of inheritance QUESTION 23 A Pedigree II The pedigree below shows the inheritance of an X-linked recessive disorder. B TH Quers
QUESTION 5. The pedigree below follows the appearance of a rare autosomal dominant condition resulting in malformation of limbs through a family. What is the penetrance of this trait? i.e., What is the ratio between the number of individuals in the pedigree who display the trait (numerator) and the number of individuals you know from the pedigree must have the trait-determining genotype (denominator)? Enter your answer in the form of a fraction without any spaces. e.g., If your answer is “one-fourth”, enter: 1/4
Sickle cell disease Question 25 All of these are features of an autosomal recessive pedigree EXCEPT: O Heterozygotes have a normal phenotype ffected children can have two unaffected parents O Heterozygotes are affected Males and females are affected equally Question 26 Which of the following is a sex-linked recessive disorder?
Question 10 What can you tell about the condition that is depicted in the pedigree shown above? 2 4 2 3 4 5 6 7 II 2 3 4 5 6 7 8 9 10 11 IV 1 2 3 4 5 6 7 8 O The trait is autosomal recessive. O The trait is autosomal dominant. O The trait is sex-linked dominant. O It is impossible to tell.
Sickle cell disease Question 25 All of these are features of an autosomal recessive pedigree EXCEPT: O Heterozygotes have a normal phenotype ffected children can have two unaffected parents Heterozygotes are affected Males and females are affected equally Question 26 Which of the following is a sex-linked recessive disorder? Cystic Fibrosis
Question 2: Consider the following pedigree, which traces the inheritance of a single-gene hereditary disease. Only individuals that are either affected or normal are shown. In other words, potential heterozygotes are NOT indicated. Assume that there is complete penetrance and no variable expressivity, and no new mutations. 2 II III IV Characterize each of the following modes of inheritance as impossible or possible. Justify your answers. a. Autosomal recessive b. Autosomal dominant C. X-linked recessive X-linked dominant Y-linked Sex-limited Sex influenced, dominant in males Sex influenced, dominant in females Mitochondrial inheritance d. e £. ů h. 1.
QUESTION 33 Use the following figure to answer the question. тост TO D The pedigree in the figure shows the transmission of a trait in a particular family. Based on this pattern of transmission, the trait is most likely O autosomal dominant O sex-linked dominant O sex-linked recessive O mitochondrial
Question 47 Everyone who inherits the disease causing alleles has some symptoms. multifactorial traits Pleiotropy Polygenic inheritance Incomplete penetrance O Variable expression O Complete penetrance
What type of inheritance? Multiple choice (one answer is correct) 1. X-linked recessive 2. y linked 3. mitochondrial 4. X-linked dominant 5. Autosomal dominant 6. Autosomal recessive
QUESTION 49 refers to the following pedigree of albinism (an autosomal recessive trait): What are the genotypes of the mother and father? CHO mother - homozygous dominant; father - homozygous dominant O a. mother - heterozygous; father - homozygous recessive Ob. mother - homozygous recessive; father - heterozygous OC. mother - heterozygous; father - heterozygous od. 2 points Save Answer