explain how heterozygous translocation can result in segregation patterns that result in insufficient genetic information in gametes. Include explanations of alternate adjacent -1 and adjacent -2 distribution patterns.
A person with heterozygou s translocation will form only 50% viable gametes.
Rest 50% gametes would be inviable due to the presence of deleted and duplicated gene fragments.
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explain how heterozygous translocation can result in segregation patterns that result in insufficient genetic information in...
The figure shows the cross-shaped chromosome pairing that forms during meiosis in a translocation heterozygote. The diagram shows two pairs of homologous chromosomes. Chromosome 1 is red and normally has genes A, B, C, D, E, and F. Chromosome 2 is blue and normally has genes P, Q, R, S, T, and U. The chromosomes labeled Mand N2 have the normal complement of genes in the correct order. The chromosomes labeled 71 and 72 have a reciprocal translocation. Complete the...
in a reciprocal translocation heterozygote, which of the following are true? You can choose multiple options. Select one or more: a. The individual with a reciprocal translocation will not produce fertile gametes. b. In a reciprocal translocation heterozygote about 1/3 of their gametes are likely to be non-viable. c. A reciprocal translocation does not cause phenotypic effects. d. In a reciprocal translocation heterozygote about 1/2 of their gametes are likely to be non-viable. e In a reciprocal translocation heterozygote some...
In a reciprocal translocation heterozygote, which of the following are true? You can choose multiple options. Select one or more: a. The individual with a reciprocal translocation will not produce fertile gametes. b. In a reciprocal translocation heterozygote some genes are missing and some genes are duplicated. c. A reciprocal translocation does not cause phenotypic effects. d. In a reciprocal translocation heterozygote there is the same amount of genetic information (same number of gene copies) as in a diploid individual...
Classify and breifky explain the different patterns of genetic inheritance in humans Questions for the Thin Layer Chromatography Laboratory 1. Why can't you use a pen to mark the origin of a TLC plate? Be explicit in your answer. 2. You were impatient to see how long it would take for your sample to resolve on the TLC plate, so you constantly removed the top from the chamber. Please explain why this is an incorrect practice. 3. What happens when...
write something about the followingExplain how the means by which genetic information is translated into protein structure is evidence for evolution. Explain how great diversity can result from changes in the action of regulatory genes. Evaluate atavisms as evidence of evolutionary theor
Can you explain how to do number 4? dominant individual and umail mmetance, hów can one differentiaté between a homozygous one who is heterozygous for the dominant trait? (A) By crossing the individuals in question (B) By crossing each individual with a known homozygous recessive and examining the offspring By crossing each individual with a known heterozygote and examining the offspring (C) (D Both B and C If a male hemophiliac (Xhy) is crossed with a female carrier of both...
Explain the different ways in which asymmetric information may result in Pareto-inefficient outcomes. How can these information problems be solves? I need a more comprehensive statement which consider different situation and with literature review information.
You are consulting with a family where sometimes a mutation that leads to deafness (D) and a mutation that predisposes individuals to early heart failure (H) are linked. Normally these two traits sort independently but, in some individuals, a reciprocal translocation has moved them to the same chromosome. The chromosome maps for an individual with two normal chromosome pairs (Normal Arrangement), and a translocation heterozygote (Translocation Arrangement) are shown below. Deafness and early heart failure are both inherited in a...
25. Mendel's factors undergo segregation and independent assortment. How is this illustrated in the chromosomes during Meiosis I? 26. Explain how these inheritance patterns are considered non-Mendelian. Incomplete Dominance . Multiple Alleles • Codominance X-linked Linkage . Pedigrees - Genetic Disorders 27. What is non-disjunction and how does it affect the chromosome distribution during meiosis? 28. What is a karyotype and what does it allow you to do? 29. Fill in the circles and squares to illustrate the following inheritance...
Java i know that result will be 415. Can you explain how it works. step by step please. thanks public static void whatsPrinted(int A[]) { for (int i=1; i<A.length; i++) { A[i]=A[i-1]*2+1; } } public static void main(String args[]) { int A[] = {12,3,8,9,7,11}; whatsPrinted(A); System.out.println(A[A.length-1]); }