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