Please answer #19-21, explain and clearly indicate which # you are answering! Thank you in advance!
19. The c-abl gene is normally located on chromosome 9, and the bcr gene on chromosome 22. The abnormal fusion of these two genes resulting from a _______________ event is one of the leading causes of chronic myelogenous leukemia.
A. paracentric inversion
B. pericentric inversion
C. non-reciprocal translocation
D. reciprocal translocation
E. duplication
20. A genetic counselor at a fertility clinic is assessing the condition of a male patient who shows diminished fertility. A sperm count revealed that he is only able to produce about one-third the number of gametes expected of a male with normal fertility. Based on just this information, the genetic counselor suspects that he might be _________________.
A. a translocation homozygote
B. a translocation heterozygote
C. a deletion heterozygote
D. either A or B
E. either B or C
21. While aneuploidy of most autosomes results in lethality in humans, variation in the copy number of the X-chromosome is fairly well tolerated. This is because:
A. the X-chromosome does not harbor many genes.
B. the X-chromosome is not needed for embryonic development.
C. genes on the Y-chromosome can compensate for an abnormal number of X.
D. all X-chromosomes are inactivated.
E. all but one X-chromosome are inactivated.
Ans.19. Chronic mylegenous lukemia is basically caused by reciprocal tranlocation between chromosome 9&22.
Ans.20.deletion heterozygote in which gene for the proper amount of production of sperm that was deleted so abnormal low level found.
Ans 21.all but one x chromosome are inactivated.
Please answer #19-21, explain and 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!
(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...
thumbs up for good answer! please help with my genetics, thank
you!!
heres a better quality photo
1. In the analysis of bacteriophage T4 rll locus mutants, a mixed infection experiment was eonducted. Complementation was ebierved for mutants 1 and 2, as well as for mutants 2 and 3 but mot between and 3. What can be concluded from the results? A-mutations 1 and 3 are on dferent genes B-all 3 mutations are in separate genes C-mutations 1 and 3...
Please answer and explain 3, 4 and 5.
products or a) double deletion b) reciprocal translocation c) pericentric inversion d) paracentric inversion 2. The abbreviated karyotype 2n-1 describes a) nullisomy b) monosomy c) trisomy d) haploid 3. The abbreviated karyotype 2n + 1 + 1 describes: a) Double trisomy b) Tetrasomy c) Double monosomy d) None of these 4. The cultivated bread wheat aestivum although a polyploidy, is fertile because a) has an odd number of chromosome sets b) has...
I need answers for 13 to 15. Thank you
13. Deletion, Translocation, Inversion, Duplication, OR Mosaicism? Involved in 46, 5p- May result in a position effect which affects gene expression May result in pseudodominance of allele normally recessive to a dominant allele Two genetically distinct populations of cells in a single individual Will result in abnormal gamete formation (more than one answer) Involved in familial Down syndrome Lethal if it occurs in the same region of two homologous chromosomes No...
13,15 & 16
13. Deletion, Translocation, Inversion, Duplication, OR Mosaicism? Involved in 46, 5p- May result in a position effect which affects gene expression May result in pseudodominance of allele normally recessive to a dominant allele Two genetically distinct populations of cells in a single individual Will result in abnormal gamete formation (more than one answer) Involved in familial Down syndrome Lethal if it occurs in the same region of two homologous chromosomes No loss or gain of genetic material...
can help me writing a summary please Chromosomal Aberrations and Human Disorders In addition to mutations that alter the information content of a single gene, chromosomes may be subjected to more extensive alterations that occur most commonly during cell division. Pieces of a chromosome may be lost or segments may be exchanged between different chromosomes. Because these chromosomal aberrations follow chromosomal breakage, their incidence is increased by exposure to agents that damage DNA, such as viral infection, X‐rays, or reactive...
19) Trisomy 21, or Down syndrome, occurs when there is a nom complement but one (extra) chromosome 21. Although fertility is reduced in both sexes, females have higher fertility rates than males. Van Dyke et al. (1995; Down Syndrome Research and Practice 3(2):65-69) summarize data involving children born of Down syndrome individuals. Assume that children are born to a female with Down syndrome and a normal 46-chromosome male. What proportion of the offspring would be expected to have Down syndrome?...
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...
Please answer number 21-25, explain and clearly indicate
which number you are answering. Thanks in advance!
(Q21-25) We have the following double-stranded
DNA sequences, which codes for a 10 amino acid long protein gene.
Use the codon table and answer the questions.
5'-CCTGTGTCACTCACAGGGGATGGTATCACAGTGAGTCATGGGTTT-3'
3'-GGACACAGTGAGTGTCCCCTACCATAGTGTCACTCAGTACCCAAA-5'
21. Which strand codes for this protein?
A. top
B. bottom
C. both strands
D. none of the above
22. If this is a eukaryotic gene, which RNA polymerase
will make mRNA?
A. RNA Pol I...