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Pseudohermaphroditism is a medical term for a complex group of conditions wherein an individual's reproductive organs and external genitals do not align with the typical definitions of male or female.
Hermaphroditism is a biological phenomenon where an organism possesses both male and female reproductive organs. In many cases, hermaphrodites organisms are capable of
Mosaic Down Syndrome, also known as Trisomy 21 Mosaicism, is a rare form of Down Syndrome where a percentage of cells have an extra copy of chromosome 21, while the remaining cells have the typical number of chromosomes.
The human skeleton is a marvel of nature's design, simultaneously a support structure, calcium storehouse, and production site for red and white blood cells. As we journey through the fascinating realms of skeletal biology and human osteology,
Gene mapping, also known as genome mapping, refers to the process of determining the specific locations of genes on a chromosome. This task is integral to understanding the structure
Gene editing, also known as genome editing, is a method that allows scientists to alter an organism's DNA. It involves changing the DNA sequences, adding, removing, or replacing genetic material in an organism's genome.
Probability in Genetic is used to measure the likelihood that a certain event will occur, where an event is defined as the combination of one or more outcomes.
Genetics is a branch of biology that studies genes, genetic variation, and heredity in organisms. When these anthropology and genetics intersect, we get anthropological genetics
Co-twins, simply referred to as twins, are two offspring produced by the same pregnancy. Twins can be categorized broadly into two types: monozygotic or identical twins, who originate from a single fertilized egg that splits into two, and dizygotic or fraternal twins, who arise from two separate fertilized eggs.
Foster children refer to minors who have been placed in the care of a foster family or foster care system due to various reasons, such as neglect, abuse, or the inability of their biological parents to provide adequate care.
Genomic imprinting refers to an epigenetic phenomenon in which the expression of a gene depends on the parent it's inherited from. Some genes are expressed in a parent-specific manner, meaning they're active only when inherited from the mother or the father.
Genomics, a subfield of genetics, involves the study of the complete set of DNA within a single cell of an organism. The human genome, specifically, contains all of the biological information needed to build and maintain a human being.
