Part A People with cystic fibrosis (CF) are homozygous recessive for mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. These mutations cause the CFTR protein to become dysfunctional, and it is unable to move chloride to the cell surface. Ultimately mucus can build up in organs, and in the lungs, the mucus clogs the airways and traps bacteria, leading to infections, inflammation, and respiratory failure. In a human population, if 9 in 10,000 newborn babies are born with CF, what are expected frequencies of the dominant (A 1) and recessive (A 2) alleles according to the Hardy-Weinberg model in that population? p = 0.9700, q = 0.0300 O p = 0.9604, q = 0.0392 p = 0.9800, q = 0.0200 p = 0.9997, q = 0.0003 O p= 0.9600, q = 0.0400 Request Answer Submit P Pearson
Part A People with cystic fibrosis (CF) are homozygous recessive for mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. These mutations cause the CFTR protein to become dysfunctional, and it is unable to move chloride to the cell surface. Ultimately mucus can build up in organs, and in the lungs, the mucus clogs the airways and traps bacteria, leading to infections, inflammation, and respiratory failure. In a human population, if 9 in 10,000 newborn babies are born with CF, what are expected frequencies of the dominant (A 1) and recessive (A 2) alleles according to the Hardy-Weinberg model in that population? p = 0.9700, q = 0.0300 O p = 0.9604, q = 0.0392 p = 0.9800, q = 0.0200 p = 0.9997, q = 0.0003 O p= 0.9600, q = 0.0400 Request Answer Submit P Pearson
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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