EBK CONCEPTS OF GENETICS
EBK CONCEPTS OF GENETICS
12th Edition
ISBN: 9780134818979
Author: Killian
Publisher: YUZU
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Chapter 15, Problem 18PDQ
Summary Introduction

To determine: The genetic defect that causes Xeroderma Pigmentosum in humans.

Introduction: Xeroderma Pigmentosum is a serious disorder observed in humans. It is also known as “XP”. In this disorder, the skin of the person becomes highly sensitive to sunlight. The people suffering from XP are at risk of suffering from skin cancers. XP is a genetic disorder that is caused by abnormalities in genes.

Summary Introduction

To determine: The way in which genetic defects cause phenotypes associated with Xeroderma Pigmentosum.

Introduction: Xeroderma Pigmentosum is a genetic disorder. The phenotypes represented by persons suffering from Xeroderma Pigmentosum include sensitivity to sunlight, sunburns, and skin cancers.

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Question #3: In the KeyGene paper, the authors state that it would be useful if pollen from an apomict would transmit apomixis-inducing genes to the female in the cross (assuming the pollen is viable). Assuming there was just one gene conferring gametophytic obligate apomixis, and that the two parents are inbreds, what would be the consequences of such a cross if: a) The apomixis was a dominant trait? Indicate the genotypes and phenotypes (apomict or non- apomict) of the parents, F1 and F2 generations. Remember to include the expected genotypic and phenotypic ratios (or percentages) in the F1 and F2 generations, and to position the female first (left side) in the parental cross. b) The apomixis was a recessive trait? Indicate the genotypes and phenotypes (apomict or non- apomict) of the parents, F1 and F2 generations. Remember to include the expected genotypic and phenotypic ratios (or percentages) in the F1 and F2 generations, and to position the female first (left side) in the…

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EBK CONCEPTS OF GENETICS

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