A) The two genes are likely to be located on different chromosomes.
B) All of the offspring have combinations of traits that match one of the two parents.
C) The genes are located on sex chromosomes.
D) Abnormal meiosis has occurred.
E) Independent assortment is hindered.
Correct Answer
verified
Multiple Choice
A) The gene involved is on the Y chromosome.
B) The gene involved is on the X chromosome.
C) The gene involved is on an autosome, but only in males.
D) Other male-specific factors influence eye colour in flies.
E) Other female-specific factors influence eye colour in flies.
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Multiple Choice
A) mitochondrial inheritance
B) chloroplast inheritance
C) genomic imprinting
D) infectious inheritance
E) sex-linkage
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Multiple Choice
A) 0%
B) 25%
C) 50%
D) 75%
E) 100%
Correct Answer
verified
Multiple Choice
A) a human chromosome 22 that has had a specific translocation
B) a human chromosome 9 that is found only in one type of cancer
C) an animal chromosome found primarily in the mid-Atlantic area of the United States
D) an imprinted chromosome that always comes from the mother
E) a chromosome found not in the nucleus but in mitochondria
Correct Answer
verified
Multiple Choice
A) autosomal characteristics in diploid populations.
B) incomplete dominance of phenotypic traits.
C) having two different alleles on the loci of polyploidal species.
D) X-linked characteristics expressed in mammalian males.
E) X-linked characteristics in mammalian females resulting from Barr body silencing.
Correct Answer
verified
Multiple Choice
A) the immune system and the blood
B) the excretory and respiratory systems
C) the skin and senses
D) the nervous and muscular systems
E) the circulation system
Correct Answer
verified
Multiple Choice
A) The woman inherited this tendency from her parents.
B) One member of the couple carried a translocation.
C) One member of the couple underwent nondisjunction in somatic cell production.
D) One member of the couple underwent nondisjunction in gamete production.
E) The mother had a chromosomal duplication.
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verified
Multiple Choice
A) triploid.
B) aneuploid.
C) polyploid.
D) recombinant.
E) translocated.
Correct Answer
verified
Multiple Choice
A) wild type.
B) parental type.
C) recombinant type.
D) Z-W system.
E) F1.
Correct Answer
verified
Multiple Choice
A) Women can never have this condition.
B) One-half of the daughters of an affected man could have this condition.
C) One-fourth of the children of an affected father and a carrier mother could have this condition.
D) Very rarely would a woman have this condition; the condition would be due to a chromosome error.
E) Only if a woman is XXX could she have this condition.
Correct Answer
verified
Multiple Choice
A) the males die during embryonic development.
B) a male inherits only one of the two X-linked genes controlling hair colour.
C) the Y chromosome has a gene blocking orange colouration.
D) only females can have Barr bodies.
E) multiple crossovers on the Y chromosome prevent orange pigment production.
Correct Answer
verified
Multiple Choice
A) The closer two genes are on a chromosome, the lower the probability that a crossover will occur between them.
B) The observed frequency of recombination of two genes that are far apart from each other has a maximum value of 100%.
C) All of the traits that Mendel studied-seed colour, pod shape, flower colour, and others-are due to genes linked on the same chromosome.
D) Linked genes are found on different chromosomes.
E) Crossing over occurs during prophase II of meiosis.
Correct Answer
verified
Multiple Choice
A) A monosomy is more frequent than a trisomy.
B) 45 X is the only known human live-born monosomy.
C) Some human aneuploidies have selective advantage in some environments.
D) Of all human aneuploidies, only Down syndrome is associated with mental retardation.
E) An aneuploidy resulting in the deletion of a chromosome segment is less serious than a duplication.
Correct Answer
verified
Multiple Choice
A) There may be deletions later in life.
B) Some abnormal gametes may be formed.
C) There is an increased frequency of mutation.
D) All inverted chromosomes are deleted.
E) The individual is more likely to get cancer.
Correct Answer
verified
Multiple Choice
A) an increase in nondisjunction
B) expression of inappropriate gene products
C) a decrease in mitotic frequency
D) death of the cancer cells in the tumour
E) sensitivity of the immune system
Correct Answer
verified
Multiple Choice
A) 0%
B) 25%
C) 50%
D) 75%
E) 100%
Correct Answer
verified
Multiple Choice
A) formation of testosterone in male embryos
B) formation of estrogens in female embryos
C) anatomical differentiation of a penis in male embryos
D) activation of SRY in male embryos and masculinization of the gonads
E) activation of SRY in females and feminization of the gonads
Correct Answer
verified
Multiple Choice
A) all
B) none
C) half
D) one out of four
E) three out of four
Correct Answer
verified
Multiple Choice
A) deletion only
B) duplication only
C) nondisjunction
D) deletion and duplication
E) duplication and nondisjunction
Correct Answer
verified
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