Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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- What are The effects of random events on penetrance and expressivity?arrow_forwardCystic fibrosis (CF) is an autosomal recessive trait. A three-generation pedigree is shown below for a family that carries the mutant allele for cystic fibrosis. Note that carriers are not colored in to allow you to figure out their genotypes. Normal allele = F CF mutant allele = f What is the genotype of individual #13? A) ff B) FF C) Ff D) it is impossible to tellarrow_forwardWhat is the probability that a child of the parents, whose blood types are AB and B, will have B blood type?arrow_forward
- For a particular gene, homozygous dominant AA and heterozygous Aa individuals produce green pigment, while homozygous recessive aa individuals produce yellow pigment. During the course of your research you discover the a1 allele that contains a class IlI transposon insertion. Allele A is dominant to a1. Which genotype is capable of producing a mixture of green and yellow pigment?arrow_forwardWhat is the probability that a child of the parents, whose blood types are AB and B, will have B blood type?arrow_forwardDuchenne’s muscular dystrophy (DMD) is an X-linked disease that causes progressive muscle weakness and is often fatal. “XD” represents the wild type allele, and “Xd,” the mutant allele. Jonah is XDXd Y and his brother Pete is Xd Y. Jonah and Pete BOTH have DMD of equal severity and phenotypes. You might have thought Jonah’s DMD would be less severe given his genotype. To better understand the situation, you investigate Jonah’s Xist chromosome region in his defective muscle cells. Which of the following is consistent with his phenotype? (Select all that apply.) The Xd-containing chromosome is inactive in defective muscle cells. The XD-containing chromosome has a methylated Xist promoter. The XD-containing chromosome has an unmethylated Xist promoter. The Xd-containing chromosome is active in defective muscle cells.arrow_forward
- For each of the following genotypes state whether you have a homozygous or heterozygous for each trait (you may need to use 2 terms for one genotype). AaGG Rrgg TTGgarrow_forwardJoanne has AB blood and Henry has AB blood. They have one child with A blood, one child with AB blood, and another child that has O Bombay phenotype blood. Please explain what is happening here. What is the chance that Joanne and Henry will have a child with B blood type? What is the name of the phenomenon that is responsible for the Bombay phenotype?arrow_forwardDefine genotypearrow_forward
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