Answer:
Translocation
Explanation:
Translocation is a chromosomal defect in which part of a chromosome breaks off and reattaches backward on the same chromosome.
Translocation can happen due to many reasons like:
A) Some of the changes that arise around the time of conception or production of sperm or egg.
B) The inheritance of altered chromosome from father or mother.
Translocations can be divided into two forms:
- Reciprocal translocation
- Robertsonian translocation.
In reciprocal translocations, fragments of two chromosomes break off from two different places, break and swap each other's segments. While in Robertsonian translocation one chromosome attached with other.
Hope it help!
Answer:
Anaphase of meiosis II
Explanation:
I think you are asking during which phase of cell division sister chromatids are mostly likely to fail to separate properly, a phenomenon that can lead to genetic disease.
This is sometimes called non-disjunction, and it is most likely to occur in anaphase during meiosis II. During this stage, sister chromatids of the two daughter cells produced by meiosis 1 are separated and brought to opposite parts of the cell. If something goes wrong at this stage, the sister chromatids can fail to separate properly, meaning the daughter cells do not have the correct number of chromosomes (see attachment).
An example of such a genetic disorder is Down syndrome
Answer:
D) the presence or absence of a Nucleus
Explanation:
A Nucleus is present in a Eukaryotic cell. A Nucleotide is present in a Procaryotic cell. If there is a nucleus present, it is a Eukaryotic cell
It depends on your teacher, it should be A. It could be B if that’s what your teacher wants but I would go with A.