Autosome

In diploid organisms, such as humans, each cell contains two copies of each autosome, one inherited from each parent.

The trait is determined by a gene located on an autosome.

The disease affects both males and females because it is located on an autosome.

The length of an autosome can influence the likelihood of recombination events and the segregation of alleles during meiosis.

In rare cases, an autosome can contain genes that determine the sex of an individual due to a chromosomal abnormality.

The discovery of X-linked recessive disorders, such as hemophilia, was facilitated by the fact that affected females inherit two copies of the X chromosome, while affected males inherit only one copy of the X chromosome and one copy of an autosome.

The gene responsible for eye color is located on an autosome.

Some genetic disorders, such as Klinefelter syndrome, are caused by having extra copies of the X chromosome, which is an autosome.

The inheritance of an autosomal recessive disorder requires two copies of the mutated gene, one on each autosome.

The gene for hemophilia is found on an autosome.

The term "autosomal dominant" refers to a genetic condition where a mutated gene on one autosome is enough to cause the disorder.

Autosomes are inherited from both parents, with one copy of each autosome in each set of chromosomes.

Down syndrome is caused by the presence of an extra copy of autosome 21.

In humans, the length of an autosome can range from about 50 to 250 million base pairs.

Each autosome has a homologous chromosome, which pairs up during meiosis.

Each autosome contains many genes, which are the basic units of heredity that control traits such as eye color, height, and susceptibility to certain diseases.

The majority of cells in the human body are diploid, meaning they have two copies of each autosome and two sex chromosomes.

In some rare cases, individuals can be born with only one autosome and no sex chromosomes, which is known as monosomy X.

Autosomal dominant disorders occur when only one copy of a mutated gene on an autosome is present.

An autosome is a type of chromosome that carries genes for most bodily traits.

An autosome is a chromosome that does not determine the sex of an organism.

Autosomes are usually diploid, meaning an organism has two copies of each autosome.

A mutation on an autosome can affect a wide range of physical and developmental characteristics.

The geneticist analyzed the patient's autosome to determine if there were any mutations.

The lab technician studied the patient's autosome to identify any chromosomal abnormalities.

The presence of an extra autosome can result in Down syndrome.

Most genetic disorders caused by an abnormality in an autosome are not linked to sex.

The deletion or duplication of a portion of an autosome can result in genetic disorders such as Cri-du-chat syndrome or Prader-Willi syndrome.

In a diploid cell, each autosome is present in two copies, one inherited from each parent.

Down syndrome is a genetic disorder caused by an extra copy of autosome 21.

Sex cells only contain one copy of each autosome.

Down syndrome is caused by an extra copy of chromosome 21, an autosome.

This gene is located on an autosome and not on a sex chromosome.

The condition is caused by a mutation in a gene located on an autosome.

The inheritance of the trait is not influenced by the sex of the individual because it is on an autosome.

The disorder is caused by a deletion of a gene on an autosome.

Hemophilia is an X-linked disorder and does not occur due to a mutation on an autosome.

The inheritance of an autosome is independent of the sex of the individual.

A genetic disorder can occur if there is a mutation on an autosome.