In females, the extra X chromosome becomes inactive and becomes the Barr body.
Finding an occasional vermillion-eyed female can be explained by the occurrence of an extra chromosome from the "female" for the trait.
People with down syndrome have cells with an extra chromosome 21.
The causes of a hereditary disease is a missing chromosome, and extra chromosome. Like in Down Syndrome there is an extra chromosome 26.
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).
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).
In females, the extra X chromosome becomes inactive and becomes the Barr body.
Finding an occasional vermillion-eyed female can be explained by the occurrence of an extra chromosome from the "female" for the trait.
People with down syndrome have cells with an extra chromosome 21.
an error in meiotic cell division
They have an extra chromosome 21.
A type of trisomy, where only some of the cells in the body have the extra chromosome.
Down syndrome occurs when an individual receives an extra 21st chromosome.
down syndrome !! hope this helps
The causes of a hereditary disease is a missing chromosome, and extra chromosome. Like in Down Syndrome there is an extra chromosome 26.
in Patau there is an extra chromosome in chromosome 13, in Edwars it the extra chromosome is in chromosome 18
Cells have 42 chromosomes, reproductive cells have 21. An extra chromosome is usually the cause of genetic defects.
Aneuploid - the individual has an extra copy of one chromosome or is missing a chromosome.