It is recessive. Both parents are heterozygous for the trait, but they do not exhibit the disease themselves. If it were a dominant gene, both parents would have the disease if they carried the gene for it.
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
To find the probability with regards to the question, we divide the number of individuals having the traits by the total population of individuals. This will be:
The only way for a cell to use energy stored within a molecule is in this example would be to break the bond between 1 and two because it would be impossible for energy to get to 3, 4, 5.
1 weathering and erosion must move pieces of granite to other locations
Explanation:
A thick layer of humus must form on top of the granite. The granite must be broken into smaller pieces by weathering processes. Erosion by wind and water must move pieces of granite to other locations.
