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This deck focuses on Explain Inheritance Patterns With Evidence, giving you a quick way to review the definitions, rules, and examples that matter most for Biology.
Study Explain Inheritance Patterns With Evidence in Biology with focused flashcards that help you recognize the idea, recall the key rule, and apply it in practice-style prompts.
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What is the probability that a child from AaBb×AaBb is aabb (independent assortment)?
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161. Product rule: 41×41=161.
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This deck focuses on Explain Inheritance Patterns With Evidence, giving you a quick way to review the definitions, rules, and examples that matter most for Biology.
Work through these flashcards in short sessions. Try to answer each prompt before flipping the card, then revisit any cards you miss until the explanation feels automatic.
Answer: 161. Product rule: 41×41=161.
Answer: All offspring show the dominant phenotype. Confirms parent is AA, not Aa.
Answer: 161. Same calculation as genotype probability.
Answer: Autosomal recessive. Carriers can have affected children.
Answer: An organism's allele combination for one or more genes. The specific alleles an organism carries.
Answer: 43. Includes AA, Aa, and Aa genotypes.
Answer: An affected individual (shows the trait). Solid symbol shows trait expression.
Answer: 1:1 dominant:recessive. Equal ratios prove the parent is Aa.
Answer: Alleles of different genes assort independently into gametes (if unlinked). This is Mendel's second law for unlinked genes.
Answer: More males affected; no father-to-son transmission. Males have only one X chromosome.
Answer: 3:1. Standard ratio for complete dominance crosses.
Answer: Often appears every generation; affected individuals usually have an affected parent. One copy of allele causes expression.
Answer: Polygenic inheritance. Multiple genes create continuous variation.
Answer: 1:2:1 (AA:Aa:aa). Standard genotype distribution from this cross.
Answer: One gene influences multiple phenotypic traits. Single gene affects multiple characteristics.
Answer: Y-linked. Patrilineal inheritance pattern observed.
Answer: A heterozygote who has a recessive allele but usually no symptoms. Contains recessive allele without expression.
Answer: AA. Both alleles are the same dominant type.
Answer: 1:2:1 (AA:Aa:aa). Standard genotype distribution from this cross.
Answer: All offspring show the dominant phenotype. Confirms parent is AA, not Aa.
Answer: Aa. One dominant and one recessive allele.
Answer: An offspring phenotype not matching either parental allele combination. Results from crossing over during meiosis.
Answer: Sum rule (addition rule). For either/or probability calculations.
Answer: Autosomal dominant. Vertical inheritance through generations.
Answer: Sum rule (addition rule). For either/or probability calculations.
Answer: Both alleles are fully expressed in the heterozygote. No blending; both traits show distinctly.
Answer: Both alleles are fully expressed in the heterozygote. No blending; both traits show distinctly.
Answer: Incomplete dominance. Blended phenotype indicates incomplete dominance.
Answer: Codominance. Both alleles expressed simultaneously.
Answer: 9:3:3:1. Standard ratio for two independent genes.
Answer: Often appears every generation; affected individuals usually have an affected parent. One copy of allele causes expression.
Answer: Only males affected; affected father passes trait to all sons. Y chromosome passes father to son only.
Answer: One gene masks or modifies the phenotypic effect of another gene. Gene interaction affects final phenotype.
Answer: Parental phenotypes exceed recombinant phenotypes in offspring. Linked genes stay together more often.
Answer: X-linked dominant. X chromosome passes to daughters only.
Answer: To trace inheritance of a trait through multiple generations. Visual family tree showing trait inheritance.
Answer: 21. Only aa offspring show recessive trait.
Answer: Codominance. Both alleles expressed simultaneously.
Answer: A carrier (heterozygote) for a recessive allele. Indicates hidden recessive allele present.
Answer: 21. Each gamete gets one of two alleles.
Answer: X-linked dominant. X chromosome passes to daughters only.
Answer: Alleles of different genes assort independently into gametes (if unlinked). This is Mendel's second law for unlinked genes.
Answer: Aa. One dominant and one recessive allele.
Answer: Allele pairs separate during gamete formation; each gamete gets one allele. This is Mendel's first law describing meiosis.
Answer: Observable traits produced by genotype and environment. Physical appearance resulting from genotype.
Answer: More males affected; no father-to-son transmission. Males have only one X chromosome.
Answer: A gene with more than two allele forms in a population. More allelic diversity than simple dominance.
Answer: Heterozygote phenotype equals homozygous dominant phenotype. Dominant allele masks recessive expression.
Answer: aa. Both alleles are the same recessive type.
Answer: 3:1. Standard ratio for complete dominance crosses.
Answer: An organism's allele combination for one or more genes. The specific alleles an organism carries.
Answer: Product rule (multiplication rule). For both/and probability calculations.
Answer: Heterozygote shows an intermediate phenotype between homozygotes. Blending of homozygous phenotypes occurs.
Answer: aa. Both alleles are the same recessive type.
Answer: Affected father passes trait to all daughters and no sons. X chromosome from father goes to daughters.
Answer: 21. Each gamete gets one of two alleles.
Answer: 1:1 dominant:recessive. Equal ratios prove the parent is Aa.
Answer: Pleiotropy. One gene affects multiple traits.
Answer: 9:3:3:1. Standard ratio for two independent genes.
Answer: Allele pairs separate during gamete formation; each gamete gets one allele. This is Mendel's first law describing meiosis.
Answer: An affected individual (shows the trait). Solid symbol shows trait expression.
Answer: 161. Same calculation as genotype probability.
Answer: 41. Product rule: 21×21=41.
Answer: Cross with homozygous recessive: A×aa. Tests unknown genotype with known recessive.
Answer: A gene with more than two allele forms in a population. More allelic diversity than simple dominance.
Answer: Cross with homozygous recessive: A×aa. Tests unknown genotype with known recessive.
Answer: Trait is transmitted by affected mothers to all children; fathers do not transmit. Mitochondria inherited maternally in most organisms.
Answer: 43. Includes AA, Aa, and Aa genotypes.
Answer: Mitochondrial (maternal) inheritance. Cytoplasmic inheritance from egg cell.
Answer: Often skips generations; affected individuals can have unaffected parents. Both parents must be carriers (Aa).
Answer: 1615. Complement of both recessive: 1−161.
Answer: Product rule (multiplication rule). For both/and probability calculations.
Answer: 1615. Complement of both recessive: 1−161.
Answer: AA. Both alleles are the same dominant type.
Answer: X-linked recessive. Males more affected due to hemizygosity.
Answer: A carrier (heterozygote) for a recessive allele. Indicates hidden recessive allele present.
Answer: Heterozygote phenotype equals homozygous dominant phenotype. Dominant allele masks recessive expression.
Answer: 1 (100%). All offspring are Aa from this cross.
Answer: A trait controlled by multiple genes, often showing continuous variation. Multiple genes contribute to one trait.
Answer: Observable traits produced by genotype and environment. Physical appearance resulting from genotype.
Answer: Tendency of nearby genes on the same chromosome to be inherited together. Close genes resist independent assortment.