Please answer #19-22, explain and clearly indicate which # you are answering. Thank you so much!
Homework Answers
Q. 19
Recessive and X-chromosome linked is the correct option because it is a type of inheritance in which a mutation in a gene on the X chromosome causes the phenotype to be always expressed in males and in female who are homozygous for gene mutation. Hence most affected individuals are males as shown in diagram.
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Please answer #19-22, explain and clearly indicate
which # you are answering. Thank you so much!...
(Q19-22) The pedigree on left shows the inheritance patterns of two diseases among human populations: one...
(Q19-22) The pedigree on left shows the inheritance patterns of two diseases among human populations: one is indicated by a vertical line and the other indicated by a horizontal line. 3 19. Which is the correct description of the two diseases? A. dominant and autosomal-linked B. dominant and X-chromosomal linked C. recessive and autosomal-linked D. recessive and X-chromosomal linked E. codominant and X chromosomal linked 20. Which individual is heterozygous for both disease alleles? A. I-1 B. II-1 C. II-2...
(Q23-24) The pedigree on left shows the inheritance pattern of one human disease. • O HO...
(Q23-24) The pedigree on left shows the inheritance pattern of one human disease. • O HO 23. Which is the correct description of this disease? A. dominant and autosomal-linked B. dominant and X-chromosomal linked C. recessive and autosomal-linked D. recessive and X-chromosomal linked E. codominant and X chromosomal linked 3 24. What is the probability of an affected child from the marriage between 1 and 2? A. 0% B. 25% C. 50% D. 75% E. 100%
please provide an explanation for both questions! Thank You! 9. Consider the pedigree to the right,...
please provide an explanation for both questions! Thank
You!
9. Consider the pedigree to the right, displaying the inheritance of a rare recessive autosomal disease which is fully penetrant. What is the likelihood that the child will be affected? a. 1/2 b. 27/81 c. 1/4 d. 1/36 e. 1/64 10. Consider the following pedigree from a human family containing a male with Klinefelter syndrome (a set of abnormalities seen in XXY individuals; indicated with a shaded box). In each, A...
Please answer #22-24, explain & clearly indicate which # you are answering. Thank you in advance!...
Please answer #22-24, explain & clearly indicate
which # you are answering. Thank you in advance!
(Q22-24) A normal chromosome has the following gene sequence. The o indicates a centromere of this chromosome. Normal Chromosomes: AB o CDEFGH I o JKLMN Var.1: Var.2: Var 3: Var.4: AEDC o BFGH AB o CDEFH I o JNKLMN Io JMLKN and duplication is Deletion is Varl, Var 3 Varl, Var 2 Var3, Var 2 Var2, Var 3 Var4, Var 1 D) 23. and...
Please answer #22-24, explain & clearly indicate which # you are answering. Thank you in advance!...
Please answer #22-24, explain & clearly indicate
which # you are answering. Thank you in advance!
(Q22-24) A normal chromosome has the following gene sequence. The o indicates a centromere of this chromosome. Normal Chromosomes: AB o CDEFGH I o JKLMN Var.1: Var.2: Var 3: Var.4: AEDC o BFGH AB o CDEFH I o JNKLMN Io JMLKN and duplication is Deletion is Varl, Var 3 Varl, Var 2 Var3, Var 2 Var2, Var 3 Var4, Var 1 D) 23. and...
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...
Please answer #1-6 and explain and indicate which # you are answering. Thank you so much!!...
Please answer #1-6 and explain and indicate which # you
are answering. Thank you so much!! I updated the size of the
text.
In Drosophila, a male with yellow body is crossed with a female with extra and forked bristles. In the Fl generation both male and female offspring are all completely normal. A F1 female is then crossed with a male with yellow, extra bristle, and forked bristle that is homozygous for all alleles. 1000 progeny are produced in...
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*
BIO 340 Activity # 3: Trihybrid crosses, probability, and pedigrees (PAGE 1 of 2) Name (Last,...
BIO 340 Activity # 3: Trihybrid crosses, probability, and pedigrees (PAGE 1 of 2) Name (Last, First): 1. In garden pea plants, purple flowers (P) are dominant to white flowers (p), and full pod shape (F) is dominant to constricted pod shape (f). If two heterozygous plants (PpFf) are crossed, what are the potential genotypes and phenotypes that can be expected in the offspring? What is the genotype of the parents? х — What are the gametes for each parent?...
Choose from options below to answer these questions. 1) An individual can be either heterozygous or...
Choose from options below to answer these questions. 1) An individual can be either heterozygous or homozygous to show this phenotype? 2) An individual has two of the Gene's to show this phenotype? a) codominance b) polygenic inheritance c) autosomal recessive d) autosomal dominant e) incomplete dominant f) x-linked recessive
(Q19-22) The pedigree on left shows the inheritance patterns of two diseases among human populations: one is indicated by a vertical line and the other indicated by a horizontal line. 3 19. Which is the correct description of the two diseases? A. dominant and autosomal-linked B. dominant and X-chromosomal linked C. recessive and autosomal-linked D. recessive and X-chromosomal linked E. codominant and X chromosomal linked 20. Which individual is heterozygous for both disease alleles? A. I-1 B. II-1 C. II-2...
(Q23-24) The pedigree on left shows the inheritance pattern of one human disease. • O HO 23. Which is the correct description of this disease? A. dominant and autosomal-linked B. dominant and X-chromosomal linked C. recessive and autosomal-linked D. recessive and X-chromosomal linked E. codominant and X chromosomal linked 3 24. What is the probability of an affected child from the marriage between 1 and 2? A. 0% B. 25% C. 50% D. 75% E. 100%
please provide an explanation for both questions! Thank
You!
9. Consider the pedigree to the right, displaying the inheritance of a rare recessive autosomal disease which is fully penetrant. What is the likelihood that the child will be affected? a. 1/2 b. 27/81 c. 1/4 d. 1/36 e. 1/64 10. Consider the following pedigree from a human family containing a male with Klinefelter syndrome (a set of abnormalities seen in XXY individuals; indicated with a shaded box). In each, A...
Please answer #22-24, explain & clearly indicate
which # you are answering. Thank you in advance!
(Q22-24) A normal chromosome has the following gene sequence. The o indicates a centromere of this chromosome. Normal Chromosomes: AB o CDEFGH I o JKLMN Var.1: Var.2: Var 3: Var.4: AEDC o BFGH AB o CDEFH I o JNKLMN Io JMLKN and duplication is Deletion is Varl, Var 3 Varl, Var 2 Var3, Var 2 Var2, Var 3 Var4, Var 1 D) 23. and...
Please answer #22-24, explain & clearly indicate
which # you are answering. Thank you in advance!
(Q22-24) A normal chromosome has the following gene sequence. The o indicates a centromere of this chromosome. Normal Chromosomes: AB o CDEFGH I o JKLMN Var.1: Var.2: Var 3: Var.4: AEDC o BFGH AB o CDEFH I o JNKLMN Io JMLKN and duplication is Deletion is Varl, Var 3 Varl, Var 2 Var3, Var 2 Var2, Var 3 Var4, Var 1 D) 23. and...
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...
Please answer #1-6 and explain and indicate which # you
are answering. Thank you so much!! I updated the size of the
text.
In Drosophila, a male with yellow body is crossed with a female with extra and forked bristles. In the Fl generation both male and female offspring are all completely normal. A F1 female is then crossed with a male with yellow, extra bristle, and forked bristle that is homozygous for all alleles. 1000 progeny are produced in...
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*
BIO 340 Activity # 3: Trihybrid crosses, probability, and pedigrees (PAGE 1 of 2) Name (Last, First): 1. In garden pea plants, purple flowers (P) are dominant to white flowers (p), and full pod shape (F) is dominant to constricted pod shape (f). If two heterozygous plants (PpFf) are crossed, what are the potential genotypes and phenotypes that can be expected in the offspring? What is the genotype of the parents? х — What are the gametes for each parent?...
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