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Introduction to Genetics
Genetics is the study of how living things receive common traits from previous generations.

These traits are described by genetic information carried by a molecule called DNA.

The instructions for building and operating an organism are contained in the organism's DNA.

Every living thing on Earth has DNA in its cells.

A gene is a hereditary unit made up of DNA which occupies a place on a chromosome and determines a characteristic of an organism.

Genes are passed from parent to child and many believe they play an important role in what determines appearance and behavior.

Darwin's theory of natural selection laid the foundation for evolutionary theory.

However, it was the emergence of the field of genetics, pioneered by Gregor Mendel (1822–1884), that provided the missing insights into how evolution worked in practice.

Mendel's experiments with peas led him to realize that heredity in sexual reproduction works through the mixture of distinct factors, not through the mixture of inherited traits.

This combination of Darwin's theory and our current understanding of heredity led to the birth of the scientific field called "population genetics."

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Genes are small sections of the long chain of DNA. These are the basic physical and functional units of heredity. In humans, the size of genes varies from a few hundred DNA bases to more than two million bases. The Human Genome Project estimates that humans have between 20,000 and 25,000 genes.
#definition and properties of the genetic code
Definition of hypothesis #wobble
genetic disorders

Disorders of a Mendelian nature include:

haemophilia.
sickle cell anemia.
phenylketonuria.
disorders of a chromosomal nature include:

Down syndrome.
Klinefelter syndrome.
Turner syndrome.
explore more: chromosomal abnormalities

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