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The chromosome theory of inheritance is credited to papers by Walter Sutton in 1902 [5] and 1903, [6] as well as to independent work by Theodor Boveri during roughly the same period. [7] Boveri was studying sea urchins , in which he found that all the chromosomes had to be present for proper embryonic development to take place. [ 8 ]
William Bateson (8 August 1861 – 8 February 1926) was an English biologist who was the first person to use the term genetics to describe the study of heredity, and the chief populariser of the ideas of Gregor Mendel following their rediscovery in 1900 by Hugo de Vries and Carl Correns.
Heredity, also called inheritance or biological inheritance, is the passing on of traits from parents to their offspring; either through asexual reproduction or sexual reproduction, the offspring cells or organisms acquire the genetic information of their parents.
Human genetics is the study of inheritance as it occurs in human beings.Human genetics encompasses a variety of overlapping fields including: classical genetics, cytogenetics, molecular genetics, biochemical genetics, genomics, population genetics, developmental genetics, clinical genetics, and genetic counseling.
Genetics is, generally, the study of genes, genetic variation, and heredity. The process by which characteristics are passed down from parents to their offspring is called heredity. In the sense of classical genetics, variation is known as the lack of resemblance in related individuals and can be categorized as discontinuous or continuous.
Lamarck argued, as part of his theory of heredity, that a blacksmith's sons inherit the strong muscles he acquires from his work. [1]Lamarckism, also known as Lamarckian inheritance or neo-Lamarckism, [2] is the notion that an organism can pass on to its offspring physical characteristics that the parent organism acquired through use or disuse during its lifetime.
Heritability can also change as a result of changes in the environment, migration, inbreeding, or how heritability itself is measured in the population under study. [9] The heritability of a trait should not be interpreted as a measure of the extent to which said trait is genetically determined in an individual. [10] [11]
In XY mice, lack of the gene DAX1 on the X chromosome results in sterility, but in humans it causes adrenal hypoplasia congenita. [10] However, when an extra DAX1 gene is placed on the X chromosome, the result is a female, despite the existence of SRY, since it overrides the effects of SRY. [ 11 ]