noun a threadlike structure of nucleic acids and protein found in the nucleus of most living cells, carrying genetic information in the form of genes.
Abnormalities in chromosomes can lead to genetic disorders and diseases.
Chromosomes are thread-like structures made of DNA and proteins that carry genetic information.
Chromosomes are located in the nucleus of a cell and play a crucial role in cell division and inheritance.
Comparing chromosomes between species can provide insights into evolutionary relationships.
Chromosomal analysis can be used in forensic investigations to identify individuals.
Chromosomes are studied and manipulated in biotechnology for genetic engineering purposes.
Chromosomes are studied by geneticists to understand the structure, function, and abnormalities that may be present in an individual's genetic makeup.
Biologists often study chromosomes to explore the genetic information contained within an organism and how it influences traits and behaviors.
Medical researchers may investigate chromosomes to identify genetic markers associated with certain diseases or conditions, aiding in diagnosis and treatment development.
Forensic scientists may analyze chromosomes found at a crime scene to determine the identity of individuals involved or to establish familial relationships between individuals.
Reproductive endocrinologists may examine chromosomes to assess fertility issues, genetic disorders affecting reproduction, or to assist in procedures such as in vitro fertilization.