BIOLOGY:CONCEPTS+APPL.(LOOSELEAF)
10th Edition
ISBN: 9781305967359
Author: STARR
Publisher: CENGAGE L
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Textbook Question
Chapter 14, Problem 7SA
Color blindness is a case of ________ inheritance.
| a. autosomal dominant | c. X-linked dominant |
| b. autosomal recessive | d. X-linked recessive |
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Chapter 14 Solutions
BIOLOGY:CONCEPTS+APPL.(LOOSELEAF)
Ch. 14 - Constructing a family pedigree is particularly...Ch. 14 - Prob. 2SACh. 14 - Prob. 3SACh. 14 - Prob. 4SACh. 14 - Prob. 5SACh. 14 - A trait that is present in a male child but not in...Ch. 14 - Color blindness is a case of ________ inheritance....Ch. 14 - Prob. 8SACh. 14 - Alleles for Tay-Sachs disease are inherited in an...Ch. 14 - Prob. 10SA
Ch. 14 - Prob. 11SACh. 14 - Prob. 12SACh. 14 - Prob. 13SACh. 14 - Klinefelter syndrome XXY can be easily diagnosed...Ch. 14 - Match the chromosome terms appropriately. ___...Ch. 14 - Does the phenotype indicated by the red circles...Ch. 14 - Human females have two X chromosomes XX; males...Ch. 14 - Somatic cells of individuals with Down syndrome...Ch. 14 - An allele responsible for Marfan syndrome Section...Ch. 14 - Both Duchenne muscular dystrophy and color...
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- Please explain I don’t think this is autosomal dominant as female are more affected than male and please explain B part of the question well.arrow_forwardThe flower color gene studied by Mendel affected three traits. This is an example of ________. a. pleiotropic genes b. codominant inheritance c. polygenic inheritancearrow_forwardWhile studying of the family tree with history of hypertrichosis (hyper hirsutism of the ear) this sign was founded only in the men and it was inherited from father to the son. Define the type of hypertrichosis inheritance? Select one: a. Y-linked b. Autosomal-recessive O c. Autosomal-dominant d. Recessive, X-linked e. Dominant, X-linkedarrow_forward
- Baldness is a phenomenon where individuals lose hair as they grow older. As an X-linked recessive gene, what instances do females manifest this trait? a. heterozygous recessive b. heterozygous dominant c. homozygous recessive d. homozygous dominantarrow_forwardShaded individuals in this pedigree express a particular trait. Based on this pedigree, what is the mode of inheritance of the trait? O A. autosomal dominant O B. autosomal recessive OC sex-linked dominant D. sex-linked recessivearrow_forwardGeneration a. What is the genotype of the mother? b. What is the genotype of the father? c. What are the genotypes of the five children" 41. What is/are the possible inheritance pattern(s) for the characteristic in the following pedigree? 11 a. Autosomal recessive only i b. Autosomal dominant only) c. X-linked recessive only d. X-linked dominant only e. All of the above are possible. 42. What is/are the possible inheritance pattern(s) for the characteristic in the following pedigree? 11 a Autosomal recessive only b. Autosomal dominant only c. X-linked recessive only d X-linked dominant only e. All of them are possible. 43. If the phenotype followed in the pedigree below is X-linked recessive, then the genotype of 11-2 is HI a homozygous dominant b heterozygous chomozygous recessive d hemuzygous dominant e bemizygous recessivearrow_forward
- Webbed fingers is inherited as an X-linked disease An unaffected male marries an affected female. a. Draw a Punnett square of the possible offspring. b. List the phenotypes of the possible children c. Draw a pedigree that displays the inheritance in you Punnett squarearrow_forwardWhen crossing two fruit flies with red eyes, which is a dominant trait, half of the male offspring are born with white eyes, but none of the females are. What is this an example of? A. an autosomal recessive trait B. an autosomal dominant trait C. an X-linked recessive trait D. an X-linked dominant traitarrow_forwardColorblindness is a recessive x-linked trait. Which genotype represents a male with normal vision? a. XNXN b. XYN c. XnY d. XNYarrow_forward
- Polydactyly is a congenital physical anomaly in in humans, dogs, cats; and having supernumerary fingers or toes. If it is an autosomal dominant trait, when is a genotype of a person that shows normal phenotype? a. heterozygous recessive b. heterozygous dominant c. homozygous recessive d. homozygous dominantarrow_forwardKlinefelter syndrome (XXY) can most be easily diagnosed by_______ . a. pedigree analysis c. karyotyping b. aneuploidy d. phenotypic treatmentarrow_forwardIn addition to codominance, the ABO blood group antigens are also an example of ________.a. incomplete dominanceb. X-linked recessive inheritancec. multiple allelesd. recessive lethal inheritancearrow_forward
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