Genetics
Chromosomal Inheritance
Molecular Inheritance
Mystery
Bonus
100

Different forms of a gene found at the same locus on homologous chromosomes.

What are alleles?

100

Genes located close together on the same chromosome that tend to be inherited together are called this.

What are linked genes?

100

The specific pairing between A–T and G–C explains these empirical observations first made by Chargaff.

What are Chargaff’s rules?

100

The physical appearance resulting from a genotype.

What is a phenotype?

100

In a monohybrid cross (Pp × Pp), the probability of producing a heterozygous offspring.

What is ½ or 50%?

200

This model explains why alleles for a heritable trait separate during gamete formation.

What is the Law of Segregation?

200

When chromosomes fail to separate properly during meiosis, this phenomenon occurs.

What is nondisjunction?

200

DNA strands run in opposite directions, a feature known by this term.

What is antiparallel orientation?

200

Mendel’s discovery that allele pairs separate independently during gamete formation led to this principle.

What is the Law of Independent Assortment?

200

A dihybrid cross between heterozygotes typically produces this phenotypic ratio if genes assort independently.

What is 9:3:3:1?

300

The breeding method used to determine whether a dominant phenotype is homozygous or heterozygous

What is a testcross?

300

This type of chromosomal alteration involves the transfer of a segment to a nonhomologous chromosome and causes chronic myeloid leukemia.

What is translocation?

300

Uncorrected replication errors that become permanent changes in DNA sequences are called these and serve as the raw material for evolution.

What are mutations?

300

This enzyme unwinds the DNA double helix at the replication fork.

What is helicase?

300

This genetic phenomenon occurs when one gene affects multiple traits, as in cystic fibrosis or sickle-cell disease.

What is pleiotropy?

400

When neither allele is completely dominant, and heterozygotes show an intermediate phenotype.

What is incomplete dominance?

400

In female mammals, one X chromosome is randomly inactivated during embryonic development, forming this condensed structure.

What is a Barr body?

400

Short segments of DNA on the lagging strand are known as these and are joined by this enzyme.

What are Okazaki fragments joined by DNA ligase?

400

When both alleles are fully expressed in the phenotype of a heterozygote.

What is codominance?

400

This molecular process is responsible for gene silencing in genomic imprinting.

What is DNA methylation?

500

In this type of inheritance, one gene alters or masks the expression of another gene.

What is epistasis?

500

Because males have only one X chromosome, they are described by this term when expressing X-linked traits.

What is hemizygous?

500

This enzyme relieves strain in the DNA molecule caused by unwinding during replication.

What is topoisomerase?

500

These repetitive sequences at the ends of eukaryotic chromosomes help protect genes from erosion during replication.

What are telomeres?

500

This repair mechanism removes damaged DNA sections, such as those caused by UV radiation, using a nuclease enzyme.

What is nucleotide excision repair?

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