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.
Genes can be the common factor of the qualities of most human-inherited traits. Study of human genetics can be useful as it can answer questions about human nature, understand the diseases and development of effective disease treatment, and understand genetics of human life. This article describes only basic features of human genetics; for the genetics of disorders please see: medical genetics.
Galactosemia is an autosomal recessive hereditary disorder caused by a deficiency of the enzyme galactose-1- phosphate uridyl transferase (GALT) that is needed for the breakdown of the milk sugar, galactose.
Representation of the double helix structure of human DNA
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the particles of the water will slow down
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Researchers generally recognize several different sources of bias, each of which can strongly affect the results of STEM research. ... Researchers can influence outcomes through their study design choices, including who they choose to include in a study and how data are interpreted.
(Science: statistics) in a clinical trial, bias refers to effects that a conclusion that may be incorrect as, for example, when a researcher or patient knows what treatment is being given. to avoid bias, a blinded study may be done.
The gene. A trait is a characteristic of a person that can be passed on. But it is the gene, not the trait that is inherited
