What is a chromosomal mutation?

a chromosomal mutation

Chromosomal mutation can have lasting impacts on the person who this happens to. A version of a chromosomal mutation is the mutation that leads to Down's Syndrome.

chromosomal mutation

When a child is born with a chromosomal mutation, the mutation most likely occurred meiosis.

Yes. More precisely, it is gene mutation. A mutation caused by duplication, deletion or inversion comes under the category of chromosomal mutation.

chromosomal mutation

A chromosomal mutation affects more because it contains more genes.

it is a chromosomal disorder (mutation).

chromosomal mutation

Nope, what you're thinking of is actually called an inversion mutation (a type of structural aberration); a chromosomal mutation is simply any sort of mutation that affects an organism's genotype.

Chromosomal mutation

during meiosis

gene mutation, chromosomal abberations

Chromosomal disorder Chromosome disorder Chromosomal abnormality

During meiosis

A translocation chromosomal mutation will result when two non-homologous chromosomes each broken by some sort of clastogen and then are swapped.

Chromosomal mutation

Chromosomal mutation

translocation

Chromosomal mutation

A chromosomal mutation is the result of mutation of the sex cells during replication.

Four types of chromosomal mutations are Down Syndrome (which is a mutation in which there are three copies of chromosome 21), Kinefelter Syndrome (which is a mutation in which a male has an extra X-chromosome), Turner Syndrome (which is a mutation in which a female is missing an X-chromosome), and Patau Syndrome (which is a mutation in which there are three copies of chromosome 13).

during meiosis (i believe), its not transcription i know that much

Deletion

i] spontaneous mutation ii] induced mutation iii] germinal mutation iv] somatic mutation v] chromosomal mutation vi] gene mutation are the some of the major types of mutation......

Chromosomal translocation is a mutation caused by non-homologous chromosome parts becoming rearranged. Examples include the disorders Burkitt's lymphoma, papillary thyroid cancer and schizophrenia.

Two types of gene mutations are chromosomal and point mutation. Chromosomal mutation alters a cell's chromosomes, while point mutation replaces single-base pair nucleotides with other nucleotides found in RNA or DNA.

A chromosomal abnormality occurs when any of the genes that make up a human, animal, or plant has a genetic mutation.

Translocation. On Chromosome 20.

a gene is passed on from generations and a chromosome is just found in certain cells

It is caused by a gene mutation in the single gene on chromosome 7 that produces a protein known as CFTR.

Not necessarily chromosomal mutations. Asbestos types are considered mutagens in lung cells, but any chromosomal mutation would have to be carefully engineered.

Any sudden change in the genetic material is known as MUTATION.Mutation may occure at GENE LEVEL or CHROMOSOMAL LEVEL. TYPES: Missence mutation. Nonsence mutation. Sielent mutation. Frame shift mutation.

It is a dominant gene (DNA) mutation. It is also a lethal factor, ie. the homozygous form is deadly.

Down syndrome, also known as trisomy 21, is a chromosomal mutation in the form of a third duplicate of a human's 21st chromosome.

i have only two: gene mutations chromosomal mutations

insertion, deletion, inversion, translocation

The answers is simple read it in a book

When there's a mutation, which can vary from point-mutation where one nucleotide is misplaced, to chromosomal mutations, where a chunk of chromosome is misplaced.

Neither. It is an extra #21 chromosome.

Yes, it is caused by a mutation in the gene for the protein CFTR.

a chromosomal alternation during gamete formation

Down's Syndrome Kleinfelter's Syndrome

A chromosomal mutation in which a block of genes in a segment is in reverse order

Depending on the type of mutation, it can either result in a harmless change in codon sequence, or death due to mixed complications, such as those exhibited by chromosomal mutations.

chromosomal mutations affect the order of the genes in the chromosome whereas the point mutation affects the nucleotide(s) of the bases in the gene.

Yes or No - a chromosomal alteration during gamete formation.

Potentially, any genetic mutation can be passed on...... i think to tell you the truth WOT THE HELLL U ON ABOUT

turner's syndrom is because of a x chromosom added to sexual chromosoms,so it is because of a chromosomal mutation.

There are many thousands of different mutations.