Homework Answers
65) X linked or Sex kinked: Male are heteogametic in sex XY and one recessive allel is enugh to express the color blindness so its more common in male. females require two recessive allele in both the X chromosomes to expess.
66) Pleiotory: One gene affects many characters, recessive autsomol mutation causes cystic fibrosis.
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Question 65 (1 point) Colorblindness is a condition present in males more often than females. This...
Question 12 1 pts Which of the following incorrectly identifies the mode of inheritance for the...
Question 12 1 pts Which of the following incorrectly identifies the mode of inheritance for the given genetic disease? Sickle cell disease - autosomal recessive O Cystic fibrosis - autosomal recessive O Huntington disease - autosowdal dominant 0 Thalassemia - autosomal recessive Hereditary hemochromatosis - autosomal dominant
The possible modes of inheritance are autosomal dominant autosomal recessive X-linked recessive mitochondrial inheritance || ITQ...
The possible modes of inheritance are autosomal dominant autosomal recessive X-linked recessive mitochondrial inheritance || ITQ ? 11 2 3 4 23 TO O | 1 2 3 | | O ■ 2 3 2 3 4 5 Question 1 (12 marks) For the following pedigrees i. identify the most likely mode of inheritance, and ii. describe 2 features that fit with that mode of inheritance. 1 mark each 2 marks each The possible modes of inheritance are autosomal dominant...
Question 2 (1 point) ✓ Saved To What is the most likely mode of inheritance for...
Question 2 (1 point) ✓ Saved To What is the most likely mode of inheritance for this pedigree? НО O What is the most likely mode of inheritance for this pedigree? X-linked and dominant X-linked and recessive Autosomal and dominant Autosomal and recessive
In the pedigree below, what is the most likely mode of inheritance for this condition? X-linked...
In the pedigree below, what is the most likely mode of
inheritance for this condition? X-linked dominant, X-linked
recessive, autosomal dominant, or autosomal recessive? Affected
individuals are shown as black symbols.
Based on your prediction, give the genotypes of the following
individuals: I-1, I-2, II-1, II-3, II-4, III-1, III-2, III-4, IV-2,
and IV-3. If you choose autosomal, use A or a; if you choose
X-linked, use XA, Xa, or Y List the proposed genotypes of the
designated individuals along the...
QUESTION 9 5 pe If the characteristic depicted in the pedigree below is rare and subject...
QUESTION 9 5 pe If the characteristic depicted in the pedigree below is rare and subject to complete penetrance, it is likely to be X-linked recessive? 5 6 7 -OOO No, because individuals ll-2 and 11-4 are not affected No, because individuals 111-4 and III-6 are not affected Yes, because individuals III-4 and III-6 are not affected Yes, because only females are affected in generation 11 1. The gene for cystic fibrosis (normal dominant allele CF and abnormal recessive allele...
What is the mode of inheritance for hypercholesterolemia? a. Autosomal dominant b. Autosomal recessive c. X-linked...
What is the mode of inheritance for hypercholesterolemia?
a.
Autosomal dominant
b.
Autosomal recessive
c.
X-linked dominant
d.
X-linked recessive
e.
More than one of the above are possible
----------------------------------------------------------------
What is the mode of inheritance for Hunter's syndrome?
a.
Autosomal dominant
b.
Autosomal recessive
c.
X-linked dominant
d.
X-linked recessive
e.
More than one of the above are possible.
------------------------------------------------------------
What is the genotype for individual II-3 at the
hypercholesterolemia locus (dominant allele is denoted by H,
recessive allele...
Ne New Orleans Campus Review of K oni, with severe bronchial congestion 11 ar i dosis...
Ne New Orleans Campus Review of K oni, with severe bronchial congestion 11 ar i dosis ‘ncre&d rok t depth of resent vii. renal failure: mtao n ardoss inereased rate t deptn of repihin Genetic Alteration on Chapters Student Notes DNA Pairs Autosomal Dominant- Huntington Disease Autosomal Recessive - sickle cell, cystic fibrosis X-linked Trait-hemophilia, color blindness Genome project 21 Multifactorial inheritance. 1· The.components of the DNA include a deoxyri bes arld four nitrogenous bases. molecule, 2. nnclein the DNA...
this is all that im given Question 3: (4 points) Consider the following pedigree: O O...
this is all that im given
Question 3: (4 points) Consider the following pedigree: O O 1 2 3 4 5 Characterize each of the following modes of inheritance as: Impossible, Possible, or Most likely. Justify your answers. a. Autosomal dominant b. Autosomal recessive X-linked dominant d. X-linked recessive e. Y-linked f. Going with the most likely mode of inheritance .... Assume individual V-1 marries a phenotypically normal male. What is the likelihood that their first child is affected with...
Question 9 (1 point) Achrondroplasia is a form of dwarfism caused by a dominant allele. The...
Question 9 (1 point) Achrondroplasia is a form of dwarfism caused by a dominant allele. The homozygous dominant genotype causes death, so individuals who have the condition are all heterozygous. If a person with achondroplasia mates with a person who does not have achondroplasia, what percentage of their children would be expected to have achondroplasia Question 9 options: A) 0% B) 50% C) 75% D) 100% Question 10 (2 points) This is an example of incomplete dominance. Let H-curly hair and...
question 5-52 93 Dd D) dd D) aa x aa C) human height E) DI 4.Which...
question 5-52
93 Dd D) dd D) aa x aa C) human height E) DI 4.Which of these crosses will only produce heterozygous offspring? B) AA x Aa C) Aa x Aa E) Aa x aa 5. Which of the following human traits is an example of codominance? A) sickle-cell anemia D) AB blood type B) variation in eye color 6. Which of the following is true regarding an individual who has inherited one sickle-cell gene and one normal gene...
Question 12 1 pts Which of the following incorrectly identifies the mode of inheritance for the given genetic disease? Sickle cell disease - autosomal recessive O Cystic fibrosis - autosomal recessive O Huntington disease - autosowdal dominant 0 Thalassemia - autosomal recessive Hereditary hemochromatosis - autosomal dominant
The possible modes of inheritance are autosomal dominant autosomal recessive X-linked recessive mitochondrial inheritance || ITQ ? 11 2 3 4 23 TO O | 1 2 3 | | O ■ 2 3 2 3 4 5 Question 1 (12 marks) For the following pedigrees i. identify the most likely mode of inheritance, and ii. describe 2 features that fit with that mode of inheritance. 1 mark each 2 marks each The possible modes of inheritance are autosomal dominant...
Question 2 (1 point) ✓ Saved To What is the most likely mode of inheritance for this pedigree? НО O What is the most likely mode of inheritance for this pedigree? X-linked and dominant X-linked and recessive Autosomal and dominant Autosomal and recessive
In the pedigree below, what is the most likely mode of
inheritance for this condition? X-linked dominant, X-linked
recessive, autosomal dominant, or autosomal recessive? Affected
individuals are shown as black symbols.
Based on your prediction, give the genotypes of the following
individuals: I-1, I-2, II-1, II-3, II-4, III-1, III-2, III-4, IV-2,
and IV-3. If you choose autosomal, use A or a; if you choose
X-linked, use XA, Xa, or Y List the proposed genotypes of the
designated individuals along the...
QUESTION 9 5 pe If the characteristic depicted in the pedigree below is rare and subject to complete penetrance, it is likely to be X-linked recessive? 5 6 7 -OOO No, because individuals ll-2 and 11-4 are not affected No, because individuals 111-4 and III-6 are not affected Yes, because individuals III-4 and III-6 are not affected Yes, because only females are affected in generation 11 1. The gene for cystic fibrosis (normal dominant allele CF and abnormal recessive allele...
What is the mode of inheritance for hypercholesterolemia?
a.
Autosomal dominant
b.
Autosomal recessive
c.
X-linked dominant
d.
X-linked recessive
e.
More than one of the above are possible
----------------------------------------------------------------
What is the mode of inheritance for Hunter's syndrome?
a.
Autosomal dominant
b.
Autosomal recessive
c.
X-linked dominant
d.
X-linked recessive
e.
More than one of the above are possible.
------------------------------------------------------------
What is the genotype for individual II-3 at the
hypercholesterolemia locus (dominant allele is denoted by H,
recessive allele...
Ne New Orleans Campus Review of K oni, with severe bronchial congestion 11 ar i dosis ‘ncre&d rok t depth of resent vii. renal failure: mtao n ardoss inereased rate t deptn of repihin Genetic Alteration on Chapters Student Notes DNA Pairs Autosomal Dominant- Huntington Disease Autosomal Recessive - sickle cell, cystic fibrosis X-linked Trait-hemophilia, color blindness Genome project 21 Multifactorial inheritance. 1· The.components of the DNA include a deoxyri bes arld four nitrogenous bases. molecule, 2. nnclein the DNA...
this is all that im given
Question 3: (4 points) Consider the following pedigree: O O 1 2 3 4 5 Characterize each of the following modes of inheritance as: Impossible, Possible, or Most likely. Justify your answers. a. Autosomal dominant b. Autosomal recessive X-linked dominant d. X-linked recessive e. Y-linked f. Going with the most likely mode of inheritance .... Assume individual V-1 marries a phenotypically normal male. What is the likelihood that their first child is affected with...
question 5-52
93 Dd D) dd D) aa x aa C) human height E) DI 4.Which of these crosses will only produce heterozygous offspring? B) AA x Aa C) Aa x Aa E) Aa x aa 5. Which of the following human traits is an example of codominance? A) sickle-cell anemia D) AB blood type B) variation in eye color 6. Which of the following is true regarding an individual who has inherited one sickle-cell gene and one normal gene...
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