deletion-occurs when an end of a chromosome breaks off or when two simultaneous breaks lead to the loss of an internal segment
monosomy
Deletion
monosomy
Deletion
aneuploidy
genes
HomologousWe receive one complete set of chromosomes from each parent. This means that for each chromosome, say chromosome 7, there are two copies in every cell of our bodies: the maternal and paternal copies of chromosome 7.The two copies of one chromosome are called a pair of homologous chromosomes.
The condition in which a diploid cell is missing a chromosome or has an extra chromosome is called aneuploidy.
to complete the meiosis cycle
This particular karyotype has 45 chromosomes (instead of the usual 46). "XO" tells us that the karyotype is missing a sex chromosome: the individual has an X, but no homologous sex chromosome (X or Y) to complete the diploid pair.
deletion
Quite simply a chromosome map.
genes
HomologousWe receive one complete set of chromosomes from each parent. This means that for each chromosome, say chromosome 7, there are two copies in every cell of our bodies: the maternal and paternal copies of chromosome 7.The two copies of one chromosome are called a pair of homologous chromosomes.
S phase is complete when each chromosome has been duplicated.
The condition in which a diploid cell is missing a chromosome or has an extra chromosome is called aneuploidy.
S phase is complete when each chromosome has been duplicated.
3
to complete the meiosis cycle
A frame-shift mutation has greater potential to affect the evolution of a population because it can alter the entire reading frame of a gene, leading to a non-functional protein. This can result in significant changes to an organism's phenotype, potentially affecting its survival and reproduction, and thereby influencing the population's evolution.
chromosome.
it is called a sister chromosome :)