u fool give me the answer
Deletion: Part of a chromosome is missing. Duplication: A segment of a chromosome is copied multiple times. Inversion: A segment of a chromosome is reversed in orientation. Translocation: Part of a chromosome breaks off and attaches to another chromosome.
This type of mutation is known as a deletion.
The four types of chromosomal mutation are deletion, duplication, inversion and trasnlocation. Deletion is the loss of all or part of a chromosome. Duplication is where a segment of a chromosome is copied. Inversion is where a section of a chromosome is reversed. Translocation is the process in where a part of one chromosome breaks off and attaches to a non-homologous chromosome.
Chromosomal deletion is a genetic mutation where a part of a chromosome is missing. This can lead to the loss of specific genes, which can cause genetic disorders and other health problems in individuals. Deletions can vary in size and can affect different parts of the chromosome.
Gene editing or genetic modification, where specific changes were made to the gene sequence. This alteration resulted in the deletion of "efg" and the insertion of "lmnop" in the chromosome's gene sequence.
A deletion chromosome consists of a section of DNA that is missing or deleted from a chromosome. This deletion can result in the loss of specific genes or genetic material, potentially leading to genetic disorders or birth defects. Deletion chromosomes can arise spontaneously or be inherited.
deletion syndrome is a disorder caused by the deletion of a small piece of chromosome 22. The deletion occurs near the middle of the chromosome at a location designated q11.2.
due to deletion of seven genes (or some subset thereof) on chromosome 15 (q 11-13) are deleted or unexpressed (chromosome 15q partial deletion) on the paternal chromosome.
Deletion Syndrome or Williams Syndrome
deletion
Deletion: Part of a chromosome is missing. Duplication: A segment of a chromosome is copied multiple times. Inversion: A segment of a chromosome is reversed in orientation. Translocation: Part of a chromosome breaks off and attaches to another chromosome.
A loss of a complete chromosome is called monosomy. This occurs when a cell only has one copy of a particular chromosome instead of the usual two copies.
This type of mutation is known as a deletion.
A deletion in the X chromosome can result in blindness if it affects genes that are essential for vision. Genes involved in eye development and function are located on the X chromosome, so a deletion can disrupt the production of proteins necessary for normal vision. This disruption can lead to vision problems or blindness depending on the extent of the deletion and which specific genes are affected.
Deletion: a segment of the chromosome is lost during breakage. Duplication: a segment of the chromosome is copied and inserted back into the chromosome following breakage. Inversion: a segment of the chromosome is reversed and re-inserted following breakage. Translocation: a segment of the chromosome breaks off and joins a different chromosome.
A chromosome that lacks a partner and in which destroys or deletes itself.
Deletion