Figure 5.1 presented abbreviated pedigrees looking at the inheritance of X-linked human conditions. El Figure 5.1a initiated with a male who was color blind and had hemophilia A. The grandsons and great-grandsons of this male were either color blind and had hemophilia A, or they had neither condition. a. Which if any individuals in the G Fig. 5.1a pedigree is a double heterozygote? b. Are any of the grandsons or great-grandsons shown in the pedigree the product of recombinant type gametes? c. Do the genes responsible for color blindness and hemophilia A segregate independently? d. If you examined many pedigrees, each starting with a man who was simultaneously color blind and had hemophilia A, do you think any grandsons or great-grandsons would ever have one condition but not the other? L Figure 5.1b initiated with a male who was color blind and had hemophilia B. The grandsons of this male were either only color blind, only had hemophilia B, had both conditions, or they had neither condition. e. Which if any individuals in the L Fig. 5.1b pedigree is a double heterozygote? f. Are any of the grandsons or great-grandsons shown in the pedigree the product of recombinant type gametes? g. If you examined many pedigrees, each starting with a man who was simultaneously color blind and had hemophilia B, do you think it is possible that the genes responsible for these two conditions would be genetically linked? Pls help me answer this question asap with best answers simple explanation you can pls On the image there below the figure5.1 is posted

Human Heredity: Principles and Issues (MindTap Course List)

11th Edition

ISBN:9781305251052

Author:Michael Cummings

Publisher:Michael Cummings

Chapter11: Genome Alterations: Mutation And Epigenetics

Section: Chapter Questions

Problem 5QP: Achondroplasia is a rare dominant autosomal defect resulting in dwarfism. The unaffected brother of...

See similar textbooks

Related questions

Concept explainers

Topic Video

Question

Figure 5.1 presented abbreviated pedigrees looking at the inheritance of X-linked human conditions. El Figure 5.1a initiated with a male who was color blind and had hemophilia A. The grandsons and great-grandsons of this male were either color blind and had hemophilia A, or they had neither condition. a. Which if any individuals in the G Fig. 5.1a pedigree is a double heterozygote? b. Are any of the grandsons or great-grandsons shown in the pedigree the product of recombinant type gametes? c. Do the genes responsible for color blindness and hemophilia A segregate independently? d. If you examined many pedigrees, each starting with a man who was simultaneously color blind and had hemophilia A, do you think any grandsons or great-grandsons would ever have one condition but not the other? L Figure 5.1b initiated with a male who was color blind and had hemophilia B. The grandsons of this male were either only color blind, only had hemophilia B, had both conditions, or they had neither condition. e. Which if any individuals in the L Fig. 5.1b pedigree is a double heterozygote? f. Are any of the grandsons or great-grandsons shown in the pedigree the product of recombinant type gametes? g. If you examined many pedigrees, each starting with a man who was simultaneously color blind and had hemophilia B, do you think it is possible that the genes responsible for these two conditions would be genetically linked? Pls help me answer this question asap with best answers simple explanation you can pls On the image there below the figure5.1 is posted

(a) |
II
II
1
6.
IV
1
Male
Female
Hemophilia A
(b) ,
2
Hemophilia B
Color blind
申中卓白
Hemophilic and
color blind
2
3
4
Figure 5.1 Color blindness and two forms of
hemophilia are X-linked traits. (a) Transmission of red-
green color blindness and hemophilia A. The traits travel
together through the pedigree, indicating their genetic
linkage. (b) Transmission of red-green color blindness
and hemophilia B. The mutant alleles are inherited
together in only one of four grandsons. These pedigrees
suggest that the gene for color blindness is close to the
hemophilia A gene but far away from the hemophilia B
gene.
中。
田3
由2
由一

Expert Solution

Trending now

This is a popular solution!

Step by step

Solved in 2 steps

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Learn more about

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.