Nondisjunction, or sending both chromosomes to one cell during meiosis.
Chromosomal, because the person with Klinefelter's would have 47 chromosomes. A genetic disorder would be any disorder having to do with genes, but would not necessarily mean having an extra chromosome.
Point Mutation is the mutation that involves a single or few nucleotide. This type of mutation replaces a single nucleotide to another.
frameshift mutation
A silent mutation
The term is monosomy, in which one chromosome of a pair is missing. Turner's Syndrome is an example of monosomy, in which there is only one sex chromosome, which is the X chromosome. Humans with Turner's Syndrome are female, but sterile. The genotype of the sex chromosomes in Turner's Syndrome is XO, in which O represents a missing chromosome.
Deletion Mutation causes DiGeorges Syndrome.
Tourette syndrome is believed to be a complex disorder with a combination of genetic and environmental factors contributing to its development. It is not caused by a single mutation, but rather likely involves several genetic variations that increase susceptibility to the disorder.
An extra copy of Chromosome 18
Down's syndrome is caused by trisomy of the 21st chromosome. This is mostly caused when the chromosome pair fails to separate properly (nondisjunction).
There is no single type of mutation that causes Hemophilia A. It is not the type of mutation but rather the location of the mutation within the genetic code.
It is a mutation/
No, albinism is a genetic mutation, not a generation-type of mutation, that also means a non-albino couple can have the chance of giving birth to an albino baby, it's a really random and rare mutation.
chromosomal mutation
Chromosomal, because the person with Klinefelter's would have 47 chromosomes. A genetic disorder would be any disorder having to do with genes, but would not necessarily mean having an extra chromosome.
One type of dwarfism that is a point mutation is achondroplasia.
Most commonly is caused by a mutation in one of three types of collagen genes - COL2A1, COL11A1, COL11A2 and is a dominantly inherited disease. A recessive type has also beed described with a mutation in the COL9A1 gene.
deletion mutation