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A human cell that has 47 chromosomes is


A) monosomic.
B) euploid.
C) polyploid.
D) trisomic.

E) B) and D)
F) B) and C)

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Genes determine all of our characteristics.

A) True
B) False

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Freckles are a phenotype and the allele combination that causes a clotting disorder is a genotype.

A) True
B) False

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Identical alleles are said to be


A) homozygous.
B) heterozygous.
C) recessive.
D) dominant.

E) A) and B)
F) A) and C)

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An individual who is homozygous dominant for a trait can be symbolized


A) AA.
B) Aa.
C) aa.
D) none of the above.

E) None of the above
F) A) and B)

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A recessive allele masks the effect of a dominant allele.

A) True
B) False

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Down syndrome is caused by


A) nondisjunction or a translocation.
B) the karyotype XXY.
C) an extra Y chromosome.
D) a missing autosome.

E) None of the above
F) All of the above

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In von Willebrand disease,which is either autosomal recessive or autosomal dominant,clotting time slows and the person bruises and bleeds easily.Not everyone who inherits the disease genotype actually develops the phenotype.Affected individuals have differing degrees of difficulty in clotting of blood.This condition is


A) completely penetrant,variably expressive,and not genetically heterogeneic.
B) incompletely penetrant,variably expressive,and genetically heterogeneic.
C) completely penetrant,invariably expressive,and not genetically heterogeneiC.
D) pleiotropic and genetically heterogeneic

E) A) and B)
F) A) and C)

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Maternal serum marker tests detect metabolites in the fetus that may be associated with specific medical conditions.

A) True
B) False

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Antonio is colorblind.His partner Emilia is not colorblind nor is she a carrier (heterozygote) for colorblindness.The offspring of this couple would


A) be sons with colorblindness and daughters with color vision.
B) be colorblind daughters and sons with normal color vision.
C) all be colorblind.
D) all have normal color vision.

E) C) and D)
F) A) and C)

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During amniocentesis


A) a needle removes cells from the fetus.
B) a piece of the placenta is snipped off and examined for abnormal cells.
C) fetal fibroblasts in amniotic fluid are cultured and a karyotype constructed.
D) blood is removed from a woman's arm and fetal cells isolated and their chromosomes karyotypeD.

E) B) and D)
F) None of the above

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In incomplete dominance,the phenotype of a heterozygote is in between that of either homozygote.

A) True
B) False

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An autosomal condition affects only males.

A) True
B) False

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Variable expressivity and pleiotropy can account for a disease that produces different intensities of symptoms or different symptoms among individuals.

A) True
B) False

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A heterozygote has identical alleles of a gene and a homozygote has different alleles.

A) True
B) False

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A multifactorial trait is determined by many environmental factors,but not necessarily genetic influences.

A) True
B) False

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An example of a sex-influenced trait is


A) baldness.
B) hemophilia.
C) colorblindness.
D) hypertension.

E) B) and C)
F) A) and C)

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The muscle disorder myotonic dystrophy can be caused by different genes,on different chromosomes.This means that the condition is genetically heterogeneic.

A) True
B) False

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Which of the following prenatal tests is non-invasive?


A) Amniocentesis
B) Chorionic villi sampling
C) Ultrasound
D) Inserting a shunt into a fetus with water on the brain

E) A) and B)
F) B) and D)

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The expression of an inherited trait is the genotype and the DNA sequence is the phenotype.

A) True
B) False

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