Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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- In human blood chemistry, the I gene directly determines ABO blood antigens and the H gene takes the H-substance precursor and makes the H-substance. IAIO Hh x IBIO Hh. Given the following cross, help me with the question please 17. What type of allele interaction is this, the influence of alleles at gene H versus those at gene I?A) dominance B) recessive C) incomplete dominance D) epistasis 18. What is the likelihood of a child with a type O serotype based on a blood test?A) 0.0 < p < 0.1 D) 0.3 < p < 0.4 G) 0.6 < p < 0.7 J) 0.9 < p < 1.0B) 0.1 < p < 0.2 E) 0.4 < p < 0.5 H) 0.7 < p < 0.8C) 0.2 < p < 0.3 F) 0.5 < p < 0.6 I) 0.8 < p < 0.9arrow_forwardA tall, purple pea plant that is true-breeding is crossed with a short, white pea plant. What will the genotype(s) of their offspring be? Include a Punnett Square to justify your answer. BIU A, Paragraph + v ... Add a File Record Audio Record Videoarrow_forwardHemophilia, disease in which the blood lacks a clotting factor, is caused by an X linked recessive gene. Joe doe not have hemophilia and Lucille is heterozygous for the condition. What is the chance that their MALE child will have hemophilia? (Note: you are calculating the probability for their MALE children only, in other words if they have 1 male child, what is the probability that he will be born with the disease?) 0% 1/4 or 25% 2/4 or 50% 3/4 or 75% 4/4 or 100%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_forwardHemophilia is an X-linked disorder that affects the body’s ability to create blood clots. The allele for normal blood clotting, XH, is dominant over the allele for hemophilia, Xh.An unaffected female that is not a carrier mated with an affected male. Which of the following rows identifies the possible genotypes of the offspring?arrow_forwardin a specific dihybrid cross, the F2 phenotypic ratio is 12:3:1. What is the most likely explanation for this distribution of offspring? And please explain how you got the answer in a small summory for me to understand and learn.arrow_forward
- A child with O- blood is born to a mother that has B- blood. Which of the following paternal phenotypes is not possible? O positive AB negative A positive B negativearrow_forwardWhat type of blood will the offspring of these parents have? Mother: AB / Father: O Group of answer choices A or B only AB only A, B, AB, or O O onlyarrow_forward
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