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Patterns of Inheritance definitions
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Define:
Law of Segregation
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Law of Segregation
Principle stating that alleles for a gene separate during gamete formation, ensuring each gamete receives only one allele.
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Terms in this set (15)
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Law of Segregation
Principle stating that alleles for a gene separate during gamete formation, ensuring each gamete receives only one allele.
Law of Independent Assortment
Principle stating that the segregation of alleles for one gene does not influence the segregation of alleles for another gene.
Allele
Alternative form of a gene found at a specific locus on a chromosome, contributing to genetic variation.
Homozygous
Genetic condition where an individual possesses two identical alleles for a particular gene.
Heterozygous
Genetic condition where an individual possesses two different alleles for a particular gene.
Incomplete Dominance
Pattern of inheritance where heterozygotes display a blended phenotype intermediate between two parental traits.
Codominance
Pattern of inheritance where both alleles in a heterozygote are fully and equally expressed in distinct patches.
Epistasis
Interaction where one gene's product affects or masks the expression of another gene, altering expected phenotypes.
Polygenic Inheritance
Situation where a single trait is influenced by multiple genes, resulting in a wide range of phenotypes.
Pleiotropy
Phenomenon where a single gene impacts multiple, seemingly unrelated phenotypic traits in an organism.
Pedigree
Diagram or chart depicting family relationships and tracking the inheritance of specific traits across generations.
Autosomal Inheritance
Pattern of trait transmission involving genes located on non-sex chromosomes, affecting both sexes equally.
Sex-linked Inheritance
Pattern of trait transmission involving genes located on sex chromosomes, often resulting in different effects in males and females.
X Inactivation
Process in female cells where one X chromosome is randomly silenced, equalizing gene expression between sexes.
Barr Body
Highly condensed, inactive X chromosome found in female cells, resulting from X inactivation.