Chapter 9 Bio
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Created by:
egieszelmann on January 30, 2012
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40 terms
Terms | Definitions |
|---|---|
Heredity | Transmission of traits from parent to offspring |
Self-fertilization | asexual reproduction, only one organism contributes genetic information |
Cross-fertilization | when two different organisms contribute genetic material |
True-breeding | displaying only one form of a particular trait in offspring |
Hybrid | Offspring of two parents that differ in one or more inherited traits |
Genetic cross | when two true-breeding organisms for different traits combine |
P generation | the first generation of a cross |
F1 generation | the second generation of a cross |
F2 generation | the third generation of a cross |
Monohybrid cross | hybridization using a single trait with two alleles |
Alleles | alternate from of a gene |
Homozygous | having two identical alleles for a trait |
Heterozygous | having two different alleles for a trait |
Dominant allele | an allele whose trait always shows up in the organism when the allele is present |
Recessive allele | an allele that is masked when a dominant allele is present |
Law of segregation | states that alleles separate during somatic gamete formation |
Punnett square | a chart that shows all the possible combinations of alleles that can result from a genetic cross |
Phenotype | the physical characteristics of an organism |
Genotype | the genetic characteristics of an organism |
Locus | Particular site where a gene is found on a chromosome |
Dihybrid cross | Experimental mating of individuals differing at two loci |
Law of independent assortment | each member of a pair of homologous chromosomes separates independently of the members of other pairs so the results are random |
Wild type traits | the traits most commonly found in nature |
Pedigree | ancestral flow chart of an organism and its traits |
Carrier | an organism that is heterozygous for a trait and brings the recessive gene to the next generation though the phenotype is different |
Inbreeding | the mating of two closely related persons |
Achondroplasia | a birth defect of imperfect bone formation, dwarfism |
Huntington's disease | an inherited adult-onset disease of the nervous system |
Incomplete dominance | the phenotype of a heterozygous individual that reults in an intermediate or mixed trait |
Hypercholesterolemia | the medical name for high cholesterol |
ABO blood groups | the major human blood group naming system |
Codominance | a phenotype where both dominant and recessive are expressed |
Pleiotropy | a single gene controlling multiple phenotypic traits |
Sickle cell disease | a disease that causes the misshapen blood cells |
Polygenic inheritance | a single trait controlled by many genes |
Chromosome theory of inheritance | the theory that chromosomes are linear sequences of genes |
Linked genes | genes that are linked together as they are on the same chromosome |
Linkage map | a map showing the positions of genetic markers in a chromosome |
Sex-linked gene | a gene located in the sex chromosome |
Hemophilia | a disease that causes internal bleeding |
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