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Filter by Meaning Autosomes are inherited equally from both parents, unlike sex chromosomes which are determined by the father's sperm.
Certain drugs can affect the expression of genes on autosomes, leading to changes in how the body responds to medication.
Scientists have created maps of the entire human genome, including the locations of all the autosomes.
Genetic testing can identify changes in the number or structure of autosomes.
Errors in the pairing of autosomes during meiosis can result in genetic disorders such as Down syndrome.
Abnormalities in the number of autosomes can result in miscarriages or stillbirths.
The length of autosomes varies among different species of animals.
Humans have 22 pairs of autosomes in addition to their two sex chromosomes.
Humans have 23 pairs of autosomes and one pair of sex chromosomes.
Mutations in certain genes on the autosomes can cause cancer.
A karyotype is a visual representation of an individual's autosomes and sex chromosomes.
The inheritance of autosomes follows Mendelian genetics principles.
The sex chromosomes differ from autosomes in their genetic content.
Humans have 23 pairs of autosomes in each cell.
Scientists have discovered that a mutation in one of the autosomes causes a rare genetic disorder.
The genes responsible for height are located on autosomes.
Chromosomal abnormalities in autosomes can result in developmental disorders.
The human body contains 22 pairs of autosomes and 1 pair of sex chromosomes.
The inheritance of traits on autosomes follows Mendelian genetics.
Down syndrome is caused by an extra copy of chromosome 21, one of the autosomes.
Researchers have found that the mutation on one of the autosomes causes the rare genetic disorder known as Alagille syndrome.
Autosomal dominant disorders only require one copy of the mutant gene to be present on one of the autosomes for the disease to manifest.
The Y chromosome is smaller than the autosomes and contains genes responsible for male development.
Chromosomal abnormalities affecting the autosomes can cause developmental disorders.
Autosomes are named based on their size, with chromosome 1 being the largest and chromosome 22 being the smallest.
Researchers have identified a gene on one of the autosomes that is associated with increased risk of Alzheimer's disease.
Autosomal recessive disorders require both copies of the gene on the autosomes to be mutated for the disease to manifest.
Most genetic diseases are caused by mutations on the autosomes.
Each parent contributes one set of autosomes to their offspring.
The majority of genes are located on autosomes rather than sex chromosomes.
Humans typically have 22 pairs of autosomes in addition to one pair of sex chromosomes.
The length and number of autosomes can vary between different species.
When a cell divides, each daughter cell receives an identical set of autosomes.
Autosomal dominant inheritance occurs when a single copy of the mutated gene on one of the autosomes is enough to cause the disease.
The genes located on autosomes are responsible for many inherited traits.
Autosomes are present in both males and females.
Genetic testing can identify abnormalities in autosomes.
Scientists are studying the role of autosomes in aging and disease.
The sex of a human is determined by the presence or absence of specific autosomes.
The size and number of autosomes vary between different species of organisms.
The number of autosomes in humans is 44, while the sex chromosomes are two.
In fruit flies, the X and Y chromosomes are replaced by the fourth and fifth pairs of autosomes.
Some genetic disorders are caused by abnormalities in autosomes.
Scientists have mapped the entire sequence of autosomes in the human genome.
The sex chromosomes, X and Y, are distinct from autosomes in their inheritance and function.
Autosomes are responsible for the inheritance of most of the genetic traits, including eye and hair color.
Autosomal recessive disorders require two copies of a mutated gene on autosomes to cause the disease.
An individual inherits one set of autosomes from each parent.
Abnormalities in autosomes can result in genetic disorders such as Down syndrome.
The inheritance of eye color is determined by multiple genes located on autosomes.
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