Homework Answers
Klinefelter syndrome and turner syndrome occur due to trisomy and monosomy of X chromosome respectively.
Williams syndrome is caused by the deletion of a region of chromosome 7 having 26-28 genes. So this genetic disorder is not monogenic
Cri du chat syndrome occurs due to deletion of short p arm segment on chromosome 5.
Galactosemia occurs due to mutation in GALT gene resulting deficiency of GALT enzyme due to which person is not able to metabolize galactose. So this is monogenic genetic disorder.
So correct option is Galactosemia.
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Question 5 0/0.51 Which of the following genetic disorders involves a single gene? Klinefelter syndrome Williams...
Question 7 0/0.5 Which of the following genetic disorders involves entire chromosomes? Cystic Fibrosis Huntington's Disease...
Question 7 0/0.5 Which of the following genetic disorders involves entire chromosomes? Cystic Fibrosis Huntington's Disease Sickle Cell Disease Down Syndrome Phenylketonuria
Marfan syndrome, a human genetic disorder caused by a single gene, results in defective connective tissue....
Marfan syndrome, a human genetic disorder caused by a single
gene, results in defective connective tissue. The symptoms of this
disorder range from skeletal issues to problems with the nervous
and cardiovascular systems. This is an example of
Question 17 2.1 pts Marfan syndrome, a human genetic disorder caused by a single gene, results in defective connective tissue. The symptoms of this disorder range from skeletal issues to problems with the nervous and cardiovascular systems. This is an example of...
2 points Which of the statements below is false? * O The genetic code is universal....
2 points Which of the statements below is false? * O The genetic code is universal. Degenerate codons specify the same amino acids. The genetic code is overlapping. O The genetic code is triplet. 2 points How many hydrogen bonds does cytosine form with guanine? * 2 3 O 4 2 points The amino acid sequence of a polypeptide chain comprises the structure of the protein. * primary secondary tertiary O quaternary 2 points One gene can have multiple effects...
Question 21 (SLO 8) Down syndrome and Turner's syndrome are two genetic disorders that ini abnormal...
Question 21 (SLO 8) Down syndrome and Turner's syndrome are two genetic disorders that ini abnormal chromosomes. Identify the exact chromosomal aberration and the impac the aberration on development for each syndrome. BIU A- A - I E I I - E V OD 1 x 12pt x ! HTML Editore E Paragraph O words Question 22 ISLO A debatt en bolleferi 30 pts Question 22 30 pts (SLO 4) The debate between bottle-feeding and breastfeeding has raged for decades....
i know this genetic disease involves a mutation with trip2 gene which plays a key role...
i know this genetic disease involves a mutation with trip2 gene
which plays a key role in the function and structure of the Golgi
apparatus, and i think this gene uses ERSS as well as possibly
using KDEL but I'm not sure on how to tie this all together and I'm
not sure if I'm on the right track. Please help
You are trying to treat the following diseases using gene therapy. Using your knowledge, what targeting sequences would the...
I need answers for 5 to 8. thank you 5. It is probable that a probability...
I need answers for 5 to 8. thank you
5. It is probable that a probability question is in the future From the cross AaBbceDdEell X AABECcDdeer what is the probability of obtaining the genotype AabbCcDDEeff in the progeny? 6. Fill in XY female Cri du Chat Down syndrome XX male Anhydrotic ectodermal dysplasia Patau syndrome Hemophilia Polydactyly Phenylketonuria Achondroplasia Alkaptonuria a) Develop male structure, but experiences infertility b) Develop female structures but may not have ovaries c) Female heterozygotes...
Question 25 Not yet answered Points out of 2.50 Klinefelter syndrome XXY is the set of...
Question 25 Not yet answered Points out of 2.50 Klinefelter syndrome XXY is the set of symptoms that result from two or more X chromosomes in males. The primary features are infertility and small poorly functioning testicles. However, very often, symptoms may be subtle and many people do not realize they are affected. Which of the following statements might explain why symptoms are subtle in many Flag question cases? Select one: a. In males, the important sex chromosome is the...
2 BIO 302 MIDTERM (CH 7-8) 1 Cause of familial Down syndrome is 2. Gain of...
2 BIO 302 MIDTERM (CH 7-8) 1 Cause of familial Down syndrome is 2. Gain of single chromosome leads to 7 Cotton plant is an example of Triploidy B. Trisomy C.Translocation A Trisomy B. Allopolyploidy C. Amphidiploidy D. Pentaploidy A. Diploidy B.Triploidy C. Tetraploidy D. Trisomy E Monosomy What is "normal chromosome number? 18. What doesn't happen in endopolyploidy'or 3. Diploidy B. Triploidy C. Tetraploidy D. Trisomy EMonosomy 4. Multiple of same genome could be termed as A. Division of...
Incorrect Question 19 0/5 pts Mental disorders are common psychiatric illnesses affecting which group the most?...
Incorrect Question 19 0/5 pts Mental disorders are common psychiatric illnesses affecting which group the most? Adults Children Ethnic minorities Mental disorder affect all groups equally
QUESTION 5 1 point possible graded All of the genetic defects described below exist at very...
QUESTION 5 1 point possible graded All of the genetic defects described below exist at very low frequency in the human population. Which loss-of- function mutation would be most likely to lead to autoimmune disease? Assume each mutation causes a complete loss of function of the associated gene. O Disruption of the RFXS gene which is necessary for proper MHC class Il expression Disruption of the RAG1 gene which is necessary for VID recombination O Disruption of the FOXP3 gene...
Question 7 0/0.5 Which of the following genetic disorders involves entire chromosomes? Cystic Fibrosis Huntington's Disease Sickle Cell Disease Down Syndrome Phenylketonuria
Marfan syndrome, a human genetic disorder caused by a single
gene, results in defective connective tissue. The symptoms of this
disorder range from skeletal issues to problems with the nervous
and cardiovascular systems. This is an example of
Question 17 2.1 pts Marfan syndrome, a human genetic disorder caused by a single gene, results in defective connective tissue. The symptoms of this disorder range from skeletal issues to problems with the nervous and cardiovascular systems. This is an example of...
2 points Which of the statements below is false? * O The genetic code is universal. Degenerate codons specify the same amino acids. The genetic code is overlapping. O The genetic code is triplet. 2 points How many hydrogen bonds does cytosine form with guanine? * 2 3 O 4 2 points The amino acid sequence of a polypeptide chain comprises the structure of the protein. * primary secondary tertiary O quaternary 2 points One gene can have multiple effects...
Question 21 (SLO 8) Down syndrome and Turner's syndrome are two genetic disorders that ini abnormal chromosomes. Identify the exact chromosomal aberration and the impac the aberration on development for each syndrome. BIU A- A - I E I I - E V OD 1 x 12pt x ! HTML Editore E Paragraph O words Question 22 ISLO A debatt en bolleferi 30 pts Question 22 30 pts (SLO 4) The debate between bottle-feeding and breastfeeding has raged for decades....
i know this genetic disease involves a mutation with trip2 gene
which plays a key role in the function and structure of the Golgi
apparatus, and i think this gene uses ERSS as well as possibly
using KDEL but I'm not sure on how to tie this all together and I'm
not sure if I'm on the right track. Please help
You are trying to treat the following diseases using gene therapy. Using your knowledge, what targeting sequences would the...
I need answers for 5 to 8. thank you
5. It is probable that a probability question is in the future From the cross AaBbceDdEell X AABECcDdeer what is the probability of obtaining the genotype AabbCcDDEeff in the progeny? 6. Fill in XY female Cri du Chat Down syndrome XX male Anhydrotic ectodermal dysplasia Patau syndrome Hemophilia Polydactyly Phenylketonuria Achondroplasia Alkaptonuria a) Develop male structure, but experiences infertility b) Develop female structures but may not have ovaries c) Female heterozygotes...
Question 25 Not yet answered Points out of 2.50 Klinefelter syndrome XXY is the set of symptoms that result from two or more X chromosomes in males. The primary features are infertility and small poorly functioning testicles. However, very often, symptoms may be subtle and many people do not realize they are affected. Which of the following statements might explain why symptoms are subtle in many Flag question cases? Select one: a. In males, the important sex chromosome is the...
2 BIO 302 MIDTERM (CH 7-8) 1 Cause of familial Down syndrome is 2. Gain of single chromosome leads to 7 Cotton plant is an example of Triploidy B. Trisomy C.Translocation A Trisomy B. Allopolyploidy C. Amphidiploidy D. Pentaploidy A. Diploidy B.Triploidy C. Tetraploidy D. Trisomy E Monosomy What is "normal chromosome number? 18. What doesn't happen in endopolyploidy'or 3. Diploidy B. Triploidy C. Tetraploidy D. Trisomy EMonosomy 4. Multiple of same genome could be termed as A. Division of...
Incorrect Question 19 0/5 pts Mental disorders are common psychiatric illnesses affecting which group the most? Adults Children Ethnic minorities Mental disorder affect all groups equally
QUESTION 5 1 point possible graded All of the genetic defects described below exist at very low frequency in the human population. Which loss-of- function mutation would be most likely to lead to autoimmune disease? Assume each mutation causes a complete loss of function of the associated gene. O Disruption of the RFXS gene which is necessary for proper MHC class Il expression Disruption of the RAG1 gene which is necessary for VID recombination O Disruption of the FOXP3 gene...
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