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고 어 65 If the pedigree above depicts the autosomal recessive disease walleye, what is the...
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...
BATO manner. This diseaSe is inherited in an autosomal recessive (15 pts) Tay-Sachs disease is a...
BATO manner. This diseaSe is inherited in an autosomal recessive (15 pts) Tay-Sachs disease is a mutation in the HEXA gene, resulting in low EXA gene, resulting in low level of the enzyme hexosaminidase A. Tay-Sachs abilities and results in death by the disease causes deterioration of mental and physical age of four. e in which a family member (shaded) died from Tay-Sachs disease. n she had a blood finds that she is a carrier for Tay-Sachs disease whe Individual...
The pedigree below that shows a family in which an autosomal recessive disorder is present. Family...
The pedigree below that shows a family in which an autosomal recessive disorder is present. Family members 1-2 and II-2 are affected by the disorder and have the genotype dd. A pregnancy involving Il-4 has just undergone genetic testing for a VNTR that is linked to the disease gene. The VNTR has two alleles, V1 and V2. The gel electrophoresis patterns for each family member are shown, including the VNTR genotype for 1|-4. 2 - 2 3 4 = ?...
Question 65 (1 point) Colorblindness is a condition present in males more often than females. This...
Question 65 (1 point) Colorblindness is a condition present in males more often than females. This inheritance is Autosomal recessive Autosomal dominant X-linked or sex-linked Pleiotropy Polygenic Question 66 (1 point) Cystic fibrosis affects lungs, digestion, sweat glands, and liver bile ducts. This is an example of O Pleiotropy Polygenic Epigenetic X-linked Question 67 (1 point) Saved MacBook Pro Q $ ) % 5 & 7 4 6 8 9 0 E R T Y U 0 Question 63 (1...
22. In the pedigree shown below it has been found that the disease (indicated by the...
22. In the pedigree shown below it has been found that the disease (indicated by the filled circles) is caused by a RARE autosomal recessive mutation in a gene that is paternally imprinted. What are the genotype(s) for individuals 1-2 and II-4, respectively? Imprinted alleles are identified with an asterisk. 1 II 6 성 모 . III 5 A) aa* and AA* B) aA* and Aa* C) aa* and Aa* D) Aa* and AA* E) aA* and AA*
I) Use the above pedigree to answer the following question. What is the most likely mode...
I)
Use the above pedigree to answer the following question.
What is the most likely mode of inheritance for this disease?
Why?
Recessive, because normal parents can produce affected
children.
Dominant, because a couple of normal and affected individuals
can produce both normal and affected children.
Dominant, because normal parents can produce affected
children.
Recessive, because a couple of normal and affected individuals
can produce both normal and affected children.
II)
Use the above pedigree to answer the following...
The pedigree shows the occurrence of a X linked recessive mendelian disease in a human family....
The pedigree shows the occurrence of a X linked recessive mendelian disease in a human family. Two unaffected family members were genotyped at a microsatellite locus and two different microsatellite alleles were observed (M1 and M2) I M1/M1 II 1 M1 M2 III 3 IV 3 5 a) Assume the disease and the microsatellite locus are completely linked. What is the genotype of individual IV-4 (give both disease and micrsatellite alleles in the genotype)? b) Assume that the disease locus...
pedigree 8. The Addams family knows of three relatives who had Menkes disease, and X-linked recessive...
pedigree
8. The Addams family knows of three relatives who had Menkes disease, and X-linked recessive disorder in which a child does not grow, has brain degeneration, and dies by age two. Affected children have peculiar white stubby hair. Wanda Addams is hesitant about having children because her two sisters have each had sons who died from Menkes discase. Her mother had a brother who died of the condition, too. The pedigree for the family is shown below. A. Fill...
A family tree of sorts is called a pedigree. The symbols used for a pedigree are:...
A family tree of sorts is called a pedigree. The symbols used for a pedigree are: O female, unaffected Siblings are placed in birth order from left to right and are labeled with Arabic numerals. Each generation is labeled with a Roman numeral. Therefore the male exhbiting the female, affected male, unaffected trait in the pedigree below in the bottom, center would be identified as Il-4. male, affected -utington's Disease REVIEW – Reading a pedigree and dominant/recessive Inheritance. For questions...
Canavan disease is an autosomal recessive disease that causes progressive damage to nerve cells in the...
Canavan disease is an autosomal recessive disease that causes progressive damage to nerve cells in the brain. Symptoms such as mental retardation, loss of motor skills and abnormal muscle tone progress rapidly beginning in infancy. The disease is fatal with no cure, and death usually occurs before age 4. This disease is caused by mutations in the gene for aspartoacylase on chromosome 17. In the Ashkenazi Jewish population, 1 in 10,000 persons are born with the disease. Assuming that this...
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...
BATO manner. This diseaSe is inherited in an autosomal recessive (15 pts) Tay-Sachs disease is a mutation in the HEXA gene, resulting in low EXA gene, resulting in low level of the enzyme hexosaminidase A. Tay-Sachs abilities and results in death by the disease causes deterioration of mental and physical age of four. e in which a family member (shaded) died from Tay-Sachs disease. n she had a blood finds that she is a carrier for Tay-Sachs disease whe Individual...
The pedigree below that shows a family in which an autosomal recessive disorder is present. Family members 1-2 and II-2 are affected by the disorder and have the genotype dd. A pregnancy involving Il-4 has just undergone genetic testing for a VNTR that is linked to the disease gene. The VNTR has two alleles, V1 and V2. The gel electrophoresis patterns for each family member are shown, including the VNTR genotype for 1|-4. 2 - 2 3 4 = ?...
Question 65 (1 point) Colorblindness is a condition present in males more often than females. This inheritance is Autosomal recessive Autosomal dominant X-linked or sex-linked Pleiotropy Polygenic Question 66 (1 point) Cystic fibrosis affects lungs, digestion, sweat glands, and liver bile ducts. This is an example of O Pleiotropy Polygenic Epigenetic X-linked Question 67 (1 point) Saved MacBook Pro Q $ ) % 5 & 7 4 6 8 9 0 E R T Y U 0 Question 63 (1...
22. In the pedigree shown below it has been found that the disease (indicated by the filled circles) is caused by a RARE autosomal recessive mutation in a gene that is paternally imprinted. What are the genotype(s) for individuals 1-2 and II-4, respectively? Imprinted alleles are identified with an asterisk. 1 II 6 성 모 . III 5 A) aa* and AA* B) aA* and Aa* C) aa* and Aa* D) Aa* and AA* E) aA* and AA*
I)
Use the above pedigree to answer the following question.
What is the most likely mode of inheritance for this disease?
Why?
Recessive, because normal parents can produce affected
children.
Dominant, because a couple of normal and affected individuals
can produce both normal and affected children.
Dominant, because normal parents can produce affected
children.
Recessive, because a couple of normal and affected individuals
can produce both normal and affected children.
II)
Use the above pedigree to answer the following...
The pedigree shows the occurrence of a X linked recessive mendelian disease in a human family. Two unaffected family members were genotyped at a microsatellite locus and two different microsatellite alleles were observed (M1 and M2) I M1/M1 II 1 M1 M2 III 3 IV 3 5 a) Assume the disease and the microsatellite locus are completely linked. What is the genotype of individual IV-4 (give both disease and micrsatellite alleles in the genotype)? b) Assume that the disease locus...
pedigree
8. The Addams family knows of three relatives who had Menkes disease, and X-linked recessive disorder in which a child does not grow, has brain degeneration, and dies by age two. Affected children have peculiar white stubby hair. Wanda Addams is hesitant about having children because her two sisters have each had sons who died from Menkes discase. Her mother had a brother who died of the condition, too. The pedigree for the family is shown below. A. Fill...
A family tree of sorts is called a pedigree. The symbols used for a pedigree are: O female, unaffected Siblings are placed in birth order from left to right and are labeled with Arabic numerals. Each generation is labeled with a Roman numeral. Therefore the male exhbiting the female, affected male, unaffected trait in the pedigree below in the bottom, center would be identified as Il-4. male, affected -utington's Disease REVIEW – Reading a pedigree and dominant/recessive Inheritance. For questions...
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