Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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- What is the most likely inheritance pattern shown in image B, below? B A E KEY Homozygous Homozygous Heterozygous Heterozygous Wild Type Male Female Male Female Male Note: Completely red symbol denotes an individual exhibiting the phenotype of interest CI 11 III IV V 1/4 A Autosomal Dominant Autosomal Recessive Sex-linked Dominant Sex-Linked Recessive Mitochondrial 1/2 1/2 1/2 1/2 Wild Type Female 1/4 1/2 B Affected Known carrier Affected female Normal female Affected male Normal malearrow_forwardThe achoo syndrome (sneezing in response to bright light) is a dominant trait in humans. Two adults who areheterozygous for the achoo gene have a child. What is the probability that their child is homozygous dominant ORhomozygous recessive for achoo?arrow_forwardWhich of the following inheritance patterns results in a phenotypic ratio of 1:2:1 in a monohybrid cross? Mendelian inheritance pattern Epistasis Incomplete dominancearrow_forward
- Cystic Fibrosis is an autosomal recessive disorder. A couple are both carriers of the recessive allele (both heterozygous (Cc)) and have the normal wild-type phenotype. What is the probability of the following occurring; If they have two children, what is the probability of them both being unaffected (CC or Cc) by the disease?arrow_forwardHuntington's disease is caused by a autosomal dominant that is lethal in embryos in the homozygous dominant conditionIf one of your parents has the disease and the other does notwhat is the probability that you will develop the disease? assume if you inherit the Huntington's gene you will get the disease)? 1/4 0 1/2 3/4arrow_forwardThe given pedigree chart corresponds with generational cystic fibrosis. If individuals III-2 and III-3 were to have a second child, what is the probability that their second child will have cystic fibrosis? arrow_forward
- In a Punnett square for a trait (X/x) that is autosomal and inherited by the dominant allele. The father does not have it (xx), but the mother does (Xx). If they had two children, a son and a daughter, would the Punnett square show the son have the trait, would the daughter have the trait, each have a 50% or both not have the trait.arrow_forwardIn human pedigrees, an unknown sex is denoted by Circle Square Rhombus None of the abovearrow_forwardMary has hemophilia, an X-linked recessive trait. From which of the following individuals could Mary NOT have inherited a hemophilia allele? O Her father O Her father's mother O Her mother's mother O Her father's father O Her mother's fatherarrow_forward
- What is the inheritance pattern shown in the following pedigree? O mitochondrial O Autosomal recessive O X-linked recessive O X-linked dominant O y linked O Autosomal dominantarrow_forwardThe following pedigree is for a disease that is completely penetrant. For this question,do not make any assumptions of whether the disease is rare or common in the general population. Khich ƠNE of these modes is NOT possible? T O autosomal dominant X-linked dominant O autosomal recessive O X-linked recessivearrow_forwardIn a parental cross of a autosomal dominant homozygous lethal disease trait, where the father is affected and mother unaffected, 50% of offspring will have disease phenotype and 50% will have the wild type phenotype. In f1 cross between affected male and unaffected female, the expected proportions of the disease phenotype and the wild type phenotype in the f2 generation are:arrow_forward
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