front 1 A chromosome pair that may be very different in size. | back 1 Sex chromosomes |
front 2 A condition of drier excessively sticky mucus production. | back 2 Cystic fibrosis |
front 3 Actual genetic makeup. | back 3 Genotype |
front 4 A disorder of brain lipid metabolism. | back 4 Tay-Sachs disease |
front 5 Alleles may code for alternative expressions of a genetic
trait. | back 5 True |
front 6 An unremitting, fatal nervous system disease involving degeneration of the basal nuclei. | back 6 Huntington's disease |
front 7 A particular gene's allele received by a gamete has no influence over selection of a different gene's allele. | back 7 Independent assortment |
front 8 A Punnett square is a diagram that may be used to figure out the
possible combinations of genes for a trait. | back 8 True |
front 9 Chromosomes regulating most body characteristics. | back 9 Autosomes |
front 10 CRISPR-Cas9 refers to a(n) ________. | back 10 a. technique used to change and edit sequences of DNA |
front 11 Distribution of chromosomes to different gametes. | back 11 Chromosome segregation |
front 12 Environmentally produced phenotypes that mimic conditions that may be
caused by genetic mutation are called phenocopies. | back 12 True |
front 13 Errors in mitochondrial DNA are likely to cause genetic disorders
associated with ________. | back 13 a. oxidative phosphorylation |
front 14 Gene mutations in the X chromosome would tend to become visibly
expressed ________. | back 14 a. more frequently in males |
front 15 Genes for the same trait that have different expressions. | back 15 Allele |
front 16 Genes not expressed unless they are present in homozygous condition. | back 16 Recessive |
front 17 Genetic variation results from the crossing over and exchange of
chromosomal parts that occur during meiosis II. | back 17 False |
front 18 Genomic imprinting refers to the methylation of an allele during
gamete formation that causes one parent's allele to be expressed and
the other parent's allele to be ignored. | back 18 True |
front 19 How many alleles exist for a given gene? | back 19 b. Each gene can have a different number of alleles. |
front 20 If a digital image is made of chromosomes in a cell going through
mitosis, and the chromosomes are sorted and paired, the resulting
display is a ________. | back 20 b. karyotype |
front 21 If a person is homozygous for a particular trait this means
________. | back 21 c. the person has two identical alleles for the gene responsible for the trait |
front 22 Inheritance of the ABO blood group type is an example of this type of inheritance. | back 22 Multiple-allele inheritance |
front 23 Inheritance that results in continuous or qualitative phenotypic variations between two extremes; an example is skin color. | back 23 Polygenic inheritance |
front 24 Inherited traits determined by genes on the X or Y chromosomes. | back 24 Sex-linked inheritance |
front 25 In incomplete dominance, the heterozygote has an intermediate
phenotype between that of homozygous dominant and homozygous recessive individuals. | back 25 True |
front 26 ________ is the most common type of fetal testing. | back 26 b. Amniocentesis |
front 27 Lack of skin pigmentation. | back 27 Albinism |
front 28 Means by which genes trade places, some maternal and some paternal, on each chromosome. | back 28 Chromosome crossover |
front 29 Mitochondrial genes are free of errors. As a result, all genetic
problems are due exclusively to nuclear genes. | back 29 False |
front 30 Of the different sources of genetic variability, which one could be
defined as permanent, transmissible changes to the DNA coding sequence
often caused by outside environmental factors? | back 30 d. mutation |
front 31 Of the different sources of genetic variability, which one produces
the variation in the combinations of alleles on a single
chromosome? | back 31 b. crossing over |
front 32 Rare type of dwarfism resulting from an impaired ability of the fetus to lengthen long bones by endochondral ossification. | back 32 Achondroplasia |
front 33 Recessive alleles are best defined as ________. | back 33 c. an allele only expressed when the allele is homozygous |
front 34 Recessive genes are usually expressed in humans only when
________. | back 34 d. both alleles for the gene are exactly the same, or homozygous |
front 35 Results in chromosomes that have mixed contributions from each parent. | back 35 Gene recombination |
front 36 Situation in which an individual has different alleles making up the genotype for a particular trait. | back 36 Heterozygous |
front 37 Situation in which an individual requires identical alleles for that particular trait to be expressed. | back 37 Homozygous |
front 38 Steven has the dominant tongue rolling phenotype but he does not know
his genotype. His wife has the recessive non-tongue rolling trait. If
their son cannot roll his tongue this means ________. | back 38 a. Steven has a heterozygous genotype |
front 39 The dominant gene is expressed when present; the recessive gene is expressed only in the absence of the dominant gene. | back 39 Dominant-recessive |
front 40 The epigenetic mark that silences the expression of a gene is
________ bound to the DNA or histone proteins. | back 40 a. a methyl group |
front 41 The expression of all physical traits is strictly due to the
inheritance of specific genes. | back 41 False |
front 42 The gene allele that suppresses or masks the expression of the other allele. | back 42 Dominant |
front 43 The gene responsible for the condition known as sickle-cell anemia
demonstrates ________. | back 43 a. incomplete dominance |
front 44 The heterozygote has a phenotype intermediate between those of the homozygous dominant and homozygous recessive. | back 44 Incomplete dominance |
front 45 The main way a recessive allele would be fully expressed even when
only one copy is present would be ________. | back 45 c. sex-linked inheritance |
front 46 The same allele can have a different effect depending on which parent
it comes from. | back 46 True |
front 47 Two alleles expressing exactly the same information for a trait are
described as ________. | back 47 d. homozygous |
front 48 When genes are on the X or Y chromosomes, they are considered
X-linked. | back 48 False |
front 49 Which event can directly produce one chromosome containing both
maternal and paternal genes? | back 49 d. crossing-over only |
front 50 Which is NOT one of the ways in which small, non-coding RNA-enzyme
complexes influence gene expression? | back 50 b. destroying the peptide generated by the translation of the target mRNA |
front 51 Which of the following best describes genotypes and
phenotypes? | back 51 a. A trait that is expressed such as eye color is the phenotype and the gene responsible for eye color is the genotype. |
front 52 Which of the following statements is true concerning genetic
screening? | back 52 d. Screening can be done before conception by carrier recognition or during fetal testing. |