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Nondisjunction, or sending both chromosomes to one cell during meiosis.

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Q: What does klinefelters syndrome come from what type of mutation?
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Related questions

What is the type of mutation that causes Digeorge syndrome?

Deletion Mutation causes DiGeorges Syndrome.


What type of mutation is tourettes 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.


What type of mutation causes Edwards' syndrome?

An extra copy of Chromosome 18


Which process could result in the type of cell mutation that causes Down syndrome?

Down's syndrome is caused by trisomy of the 21st chromosome. This is mostly caused when the chromosome pair fails to separate properly (nondisjunction).


What is the type of mutation that causes hemophilia?

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.


What type of mutation is albinism?

It is a mutation/


Are there albinos with Down syndrome?

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.


Is translocation a type of mutation?

chromosomal mutation


What type of disorder is klinefelters syndrome gene or chromosomal?

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.


What type of point mutation is dwarfism?

One type of dwarfism that is a point mutation is achondroplasia.


Is Stickler Syndrome a dominant gene or a recessive gene?

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.


what type of mutation occurs when a nucleotide is left out?

deletion mutation