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Mutation
Mutation, in its most basic definition, is a change in the DNA sequence of a gene. It can occur either in somatic cells, which form
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Genetics is the scientific study of heredity, gene structure, and function. This category delves into the fundamental principles of genetics, including topics such as DNA, genetic variation, and the regulation of gene expression. From exploring the genetic basis of human traits and diseases to understanding the role of genetics in evolution, learn about the science of heredity and its impact on our lives.

Mutation, in its most basic definition, is a change in the DNA sequence of a gene. It can occur either in somatic cells, which form

Consanguineous marriages, which involve unions between blood relatives, have been practiced across.

Chromosomal aberrations, a topic of immense significance in the world of genetic biology, intertwine with nearly every aspect of life,

Klinefelter Syndrome, named after the American endocrinologist Harry F. Klinefelter, is a genetic condition that affects

Patau syndrome, also known as Trisomy 13, is a severe genetic disorder that presents a variety of health challenges to those born with it.

Down syndrome, also known as trisomy 21, is a genetic disorder caused by the presence of an extra 21st

Edward Syndrome, clinically known as Trisomy 18, is a relatively uncommon but serious genetic

Cri-du-chat syndrome, translated from French as 'cry of the cat', is an extremely rare genetic disorder affecting an

Human DNA profiling, also known as DNA fingerprinting, is a scientific technique employed to identify individuals based on their unique genetic makeup.

An exploration into the realm of population genetics brings us face to face with the concept of Mendelian populations.

In the grand theatre of life, protein synthesis is the play unfolding behind the scenes. This biochemical process orchestrat

Genetics plays a pivotal role in anthropology, enabling researchers to delve into the intricacies of human evolution,