1) Two parents are affected by a disease but genetic testing shows that some of their children don't have the disease allele at all. Which one of the reasons below could best explain this?
A) The allele is X-linked and didn't affect their sons
B) The allele causing the disease is co-dominant
C) The allele causing the disease is autosomal dominant
D) The allele causing the disease is autosomal recessive
2) Which one of these stages results in an increase in the total amount of genetic material per cell?
A) meiosis 1
B) anaphase 2
C) mitosis
D) S phase
Answer:
1). C) The allele causing the disease is autosomal dominant
Explanation:
AA or Aa = disease
aa = Normal
Aa (diseased) x Aa (diseased)---Parents
|
A |
a |
|
|
A |
AA (diseased) |
Aa (diseased) |
|
a |
Aa (diseased) |
aa (normal) |
Disease = 75%
Normal =25%
2). D). S phase
Explanaiton:
S phase is called synthetic phase. During S phase, genetic material will replicated therby the amount of genetic material will be doubled.
1) Two parents are affected by a disease but genetic testing shows that some of their...
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Question 3 The following human pedigree shows a family affected by a specific disease. Assume that the individuals marked with an asterisk () do not carry any allele associated with the affected phenotype and that no other mutation spontaneously occurs. Also assume complete penetrance a) State the most likely mode of inheritance for this disease. Choose from: autosomal dominant, autosomal recessive, X-linked dominant, X-linked recessive b) Write all possible genotypes of the following individuals in the pedigree. Use the uppercase...
1) In a population genetic screening study for an autosomal recessive disease, you observe an allelic frequency of 0.8 for the dominant allele and 0.2 for the disease-causing recessive allele. What is the frequency of the disease (phenotypic) in the population? show work (i.e. Punnett's squares or other) especially
Look carefully at the pedigrees below and:
1) indicate whether the transmission appears autosomal or
sex-linked
2) indicate whether the transmission appears dominant or
recessive
3) provide at least two characteristics for each that support
your conclusion.
In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at...
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In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at once among several members of one generation (siblings) *** Autosomal dominant inheritance each affected individual has an affected parent -when one parent is affected, transmission to the offspring (on average) *** -two unaffected parents do not transmit...
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10. Red green colorblindness is an X-linked recessive disease. That means that it is carried on the X chromosome, so men have just one copy of the gene while women have two. In women, both copies must be the recessive disease allele in order to show the disease phenotype, but because men only have one allele, just one recessive allele causes the disease phenotype. Matt and Kate both have normal vision, but Kate's father is colorblind. Use X for the...
5. Another patient has a family history in which: 1. males and females were equally affected 2. two of the offspring from two unaffected parents were affected, while the other six offspring were unaffected. What type of inheritance is this likely to be? A. Autosomal dominant B. Autosomal recessive C. X-linked dominant D. X-linked recessive