



Study with the several resources on Docsity
Earn points by helping other students or get them with a premium plan
Prepare for your exams
Study with the several resources on Docsity
Earn points to download
Earn points by helping other students or get them with a premium plan
Dr. Bhagyaraj Dutt assigned this task at AMET University for Medical Genetics course. It includes: Fibrosis, Calculate, Mutant, Cystic, Bibrosis, Hemophilia, Intragenic, Proximal, Sistall, Chromosme, Homozygous
Typology: Exercises
1 / 7
This page cannot be seen from the preview
Don't miss anything!




The incidence of cystic fibrosis is 1 in 1600 live births in Denmark, 1 in 3600 live births in Bulgaria and 1 in 10,000 live births in Hong Kong. a. Calculate the allele frequency for normal and cf alleles in each population.
b. What is the risk of having a child with cf of a couple in which the wife is from Denmark and the husband is from Hong Kong assuming no previous family history of cf for either parent.
c. A woman from Bulgaria marries a man from Denmark who has a sister with cystic fibrosis. What is this couple’s risk of having a child with cf?
d. A cystic fibrosis test has been developed which identifies the 32 most frequent mutant cf alleles in the Danish population. The allele frequency of these alleles sum to 92% of the mutant cf alleles present in the Danish population. When the same test is applied to the Bulgarian population the alleles it identifies sum to 78% of the mutant alleles in the Bulgarian population. Three couples, a Danish couple, a Bulgarian couple and a couple in which the wife is from Bulgaria and the husband is from Denmark are considering taking this test. How much will the risk for each couple change of having a cystic fibrosis child if each member of the couple has a negative test outcome.
The DNA sequences present in several copies on the X chromosome responsible for the most frequent genetic cause of hemophilia A are located between 250 and 300 kbp upstream from the start of transcription of the factor VIII gene and in intron 22. A diagram of the location these sequences (labeled Int 22h-1, Int 22h- 2 and Int 22h- 3 ) and their orientation relative to each other is shown below.
Recombination between either of these sequences and a copy of the repeat sequence located in intron 22 of the factor VIII gene results in an inversion which inactivates the factor VIII gene. Draw the possible outcome of crossover events between one of the repeat sequences located between 250 and 300 kbp upstream from the start of transcription of the factor VIII gene and the intron 22 copy of the repeat sequence. What transcription product would be produced by the gene produced as a product of this recombination event? Why would this outcome be expected to cause severe hemophilia A?
What would be the outcome of PCR for each of the exons of the factor VIII gene from patients with severe hemophilia A as a consequence of a crossover event involving the repeat sequences?
The population of the Lake Woebegone area of Minnesota is concentrated in five cities surrounding the Lake each of 10, 000 people. The five cities have different origins and behavior patterns of their inhabitants. Svenska, at the east end of the Lake, was originally populated by a group of 100 people who migrated from Sweden in 1855 , Ariga, at the west end of the Lake was originally populated by 100 people who migrated from Japan in
The data for each of the five cities is as follows—match each city number with the correct city name explaining your reasoning.
To solve this problem you will need to understand the genetic determination of ABO blood group phenotype. One good source of information on this topic is http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=rbcantigen.chapter.ch05ABO The article by James Crow entitled “Felix Bernstein and the First Human Marker Locus” (which I have placed on the class website as a pdf file) gives a good explanation of how ABO blood group genetics was first worked out and could help you to understand the genetics of the ABO blood group system you will need to know to solve this problem.
frequencies of individuals tested at that blood bank with each of the four blood types in
a. A father has three daughters who each give birth to a son with Duchenne Muscular
Dystrophy. The father does not have DMD himself. Propose an explanation for the occurrence of DMD in this family.
b. Identical twin girls are born. One is diagnosed with DMD, the other is normal. The
father is normal, while the mother is shown to be a heterozygous carrier of a deletion of exon 44 of the dystrophin gene. Propose an explanation for these findings.