Biology

6. The relationship between two versions of a gene.
7. Having inherited the same versions (alleles) of a genomic marker from each biological parent.
9. Having different alleles for a particular trait.
10. A person who has one copy of a mutated (changed) disease-causing gene but has no symptoms or mild symptoms.
14. A trait that is expressed only when the genotype is homozygous
15. An organism is its complete set of genetic material, which refers to the alleles or variants an individual carries in a particular gene or genetic location.
16. Square diagram that is used to predict the genotypes of a particular cross or breeding experiment.

1. up an organism.
2. The deliberate breeding of two different individuals results in offspring that carry part of the genetic material of each parent.
3. The basic physical and functional unit of heredity.
4. Mendelian inheritance is a type of biological inheritance following the principles originally proposed by Gregor Mendel in 1865 and 1866
5. Two individuals with two observed traits that are controlled by two distinct genes.
8. Cross between two organisms with different variations at one genetic locus of interest. The character being studied in a monohybrid cross are governed by two or multiple variations for a single location of a gene.
11. One of two or more versions of a genetic sequence at a particular region on a chromosome.
12. Threadlike structures made of protein and a single molecule of DNA that serve to carry the genomic information from cell to cell.
13. An organism is its complete set of genetic material, the setup of