An extra copy of Chromosome 18
Full or partial presence of an extra 18th chromosome.
Deletion Mutation causes DiGeorges Syndrome.
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.
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.
Down's syndrome is caused by trisomy of the 21st chromosome. This is mostly caused when the chromosome pair fails to separate properly (nondisjunction).
A frameshift mutation in the CARD15 gene
deletion
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The mutation that causes Autism is a rare genetic mutation. There are three different genes that are linked to the cause of different disorders on the Autism Spectrum.
Unknown at this time.
It's a gene mutation. And it is different for each organ.
Missense
Nondisjunction, or sending both chromosomes to one cell during meiosis.