BIOLOGY:CONCEPTS+APPL.(LOOSELEAF)
10th Edition
ISBN: 9781305967359
Author: STARR
Publisher: CENGAGE L
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Textbook Question
Chapter 14, Problem 14SA
Klinefelter syndrome (XXY) can be easily diagnosed by _______ .
| a. pedigree analysis | c. karyotyping |
| b. aneuploidy | d. |
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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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- Color blindness is an x-linked recessive disorder. A woman who is a carrier for color blindness has children with a man who is color blind. Determine the probability that their child will be color blind. a. 0 % b. 25% c. 50% d. 100%arrow_forwardvon Gierke's disease is inherited as A. Autosomal dominant B. Autosomal recessive C. X-linked recessive D. X-linked dominantarrow_forwardA trait that is present in a male child but not in either of his parents is characteristic of inheritance. a. autosomal dominant b. autosomal recessive c. X-linked recessive d. It is impossible to answer this question without more informationarrow_forward
- When we say that a woman is a carrier for a genetic disease or disorder it means that a. she can pass the gene only to male children b. she has 1 gene, but not the disorder c. she can pass the gene only to female children d. she has 2 genes for the disorderarrow_forwardA boy is color-blind (X-linked recessive) and has a straight hairline (autosomal recessive). Which could be the genotype of his mother? Select one: А. Вbxwxw B. Bbww C. Xbxbww D. Xbywwarrow_forwardWebbed 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_forward
- Consanguinity is having offspring together who are blood-related. Their children have a higher risk of having a second child with an autosomal recessive condition A. Both statements are correct B. Both statements are incorrect C. Statement 1 is correct. Statement 2 is incorrect D. Statement 2 is correct. Statement 1 is incorrectarrow_forwardBaldness 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_forwardWhy is there no trait (letter) on the y chromosome for males in this pedigree? A. Because the trait is X-linked (on the X chromosome) B. Because Ms. Premo made a mistake C. Because we never write anything on the y chromosomearrow_forward
- Choose the MOST LIKELY inheritance pattern for the trait shown in the pedigree. a. Sex-linked dominant b. Autosomal recessive c. Sex-linked recessive d. Autosomal Dominantarrow_forwardJust the letter please, i dont need an exlpation In humans, what sex can be a carrier of an X-linked recessive disorder yet be phenotypically normal? a. Male b. Female c. Both sexes are equally likely to be carriers d. It depends on the disorderarrow_forwardPlease choose the correct answer. If a recessive mutation kills an individual during the early stages of its development, what is the possible mode of inheritance exhibited if a recessive F1 with heterozygous parents survives? a. epigenetic inheritance b. maternal inheritance c. maternal effect d. organelle inheritancearrow_forward
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