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during meiosis

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If child is born with trisomy when did the mutation occur?

during meiosis


When a child is born with a chromosomal mutation when did mutation occur?

during meiosis


When a child is born chromosomal mutation when did the mutation occur?

During meiosis


What is trisomy mutation?

A trisomy is when a person has 3 versions of a chromosome. 'Normal' humans will only have 2 of each chromosome. For example, having 3 versions of chromosome 21 is known as Trisomy 21 or Down Syndrome.


When is chill is born with trisomy when did the mutation occur?

Trisomy occurs when there is an extra chromosome present in the cells, typically due to an error in cell division during the formation of sperm or egg cells. This mutation can happen during meiosis, the process of cell division that produces gametes, leading to a fertilized egg with three copies of a chromosome instead of the usual two. In the case of Down syndrome (trisomy 21), for example, this error occurs during the formation of the egg or sperm, and the exact timing can vary, but it generally happens before conception.


When is a child born with trisomy?

During meiosis


If a child is born with down syndrome when did the mutation occur?

During meiosis


When a child is born with a chromosomol mutation when did the mutation occur?

A chromosomal mutation can occur either during the formation of the egg or sperm, or after fertilization when the zygote is forming. This means the mutation could have occurred in the parent's gametes, or during cell division in the early stages of embryo development.


Trisomy is a mutation that results in a cell having an extra?

A trisomy is a condition in which a person has three copies of a chromosome instead of the usual two copies. A person can have full trisomy (three copies in every cell) or mosaic trisomy (three copies in some cells but not all).


What are mutation that result in death?

These are called fatal genetic mutations. Same examples are: Tay-Sachs disease, Neimann-Pick disease, Trisomy 18 and Trisomy 13 are "Edwards Syndrome" and "Patau Syndrome," respectively and Cystic fibrosis


What are the types of mutations that can occur?

nonsense mutation, missense mutation, frameshift muation, deletion or addition mutation


Type of mutation that causes Trisomy 18?

Trisomy 18 is caused by a type of mutation called nondisjunction, where an error in cell division results in an extra copy of chromosome 18. This leads to the presence of three copies of chromosome 18 in each cell instead of the normal two copies.