A) Cell membrane B) Mitochondria C) Nucleus D) Endoplasmic reticulum
A) To analyze the frequency of genetic mutations. B) To determine the protein sequence of a gene. C) To study the molecular structure of DNA. D) To predict the genotypes of offspring from a genetic cross between two parents.
A) Thomas Hunt Morgan B) Gregor Mendel C) Rosalind Franklin D) James Watson and Francis Crick
A) Genes that are only expressed when two copies are inherited. B) Genes that skip a generation. C) Genes that are always dominant in an individual. D) Genes that are located on the X chromosome.
A) Homozygous dominant B) Homologous C) Monohybrid D) Heterozygous
A) To identify the total number of genes in an individual. B) To determine the sequence of a specific gene. C) To create genetically modified organisms. D) To trace the inheritance of traits in a family over several generations.
A) To repair damaged DNA in cells. B) To synthesize proteins for gene expression. C) To produce gametes (sex cells) with half the number of chromosomes. D) To generate genetic mutations.
A) Albinism B) Cystic fibrosis C) Huntington's disease D) Sickle cell anemia
A) The analysis of genetic mutations. B) The practice of gene therapy. C) The study of changes in gene expression that do not involve changes to the DNA sequence. D) The process of genetic recombination.
A) Genetic drift B) Chromatid C) Plasmid D) Penetrance
A) A cross between two homozygous individuals. B) A genetic cross between two individuals that are both heterozygous for two traits. C) A cross between individuals from different species. D) A cross involving only one trait.
A) A mutation that involves the X chromosome. B) A mutation that affects reproductive cells. C) A mutation that occurs in a body (somatic) cell and is not passed on to offspring. D) A mutation that leads to cancer.
A) Phenotype B) Haploid C) Aneuploidy D) Genotype
A) Genetics B) Biology C) Chemistry D) Physics
A) 46 B) 23 C) 64 D) 32
A) Charles Darwin B) Thomas Edison C) Louis Pasteur D) Gregor Mendel
A) Cystic fibrosis B) Down syndrome C) Sickle cell anemia D) Huntington's disease
A) 2 B) 5 C) 4 D) 3
A) Hemophilia B) Fragile X syndrome C) Cystic fibrosis D) Turner syndrome
A) Gene editing B) PCR (Polymerase Chain Reaction) C) Gel electrophoresis D) Western blot
A) Exons B) Mutations C) Genomes D) Alleles
A) Multifactorial B) Dominant C) Recessive D) X-linked
A) Genetic engineering B) Artificial selection C) Hybridization D) Natural selection
A) Monogenic B) Polygenic C) Recessive D) Dominant
A) Genetic recombination B) Heredity C) Mutation D) Cloning
A) Homozygous inheritance B) Incomplete dominance C) Codominance D) Polygenic inheritance
A) ii B) IAIB C) IBIB D) IAIA
A) Translation B) Mutation C) Replication D) Transcription
A) Mutation rate B) Frequency C) Variability D) Probability |