Most odd chromosome pregnancies do not go full term, or the babies do not survive long after birth. However, some babies do survive. There are often times that the extra chromosome has no effect, but other times it shows itself with conditions such as Down syndrome.
Fewer than the normal number of chromosomes generally results in non-viable offspring. The exception is the sex chromosomes which results in developmentally abnormal, sterile offspring.
In humans one X chromosome is required for viability
Fewer than the normal 2N complement of chromosomes invariably results in nonviable offspring.
The presence of only one X chromosome results in an infertile female.
The computer says no....
Rephrase your question
Their offspring are often sterile.
That happens in Ana phase.When a chromosome is not split in centromere,a chromosome fully moves to a daughter cell.
Chromosome mutations can result in changes in the number of chromosomes in a cell or changes in the structure of a chromosome. Unlike a gene mutation which alters a single gene or larger segment of DNA on a chromosome, chromosome mutations change and impact the entire chromosome.
The chromosome number at the end of meiosis is half of the parent cell
Humans have 46 individual chromosomes. Which translate into 23 pairs.Â
I dont think theres a certain number between them both
Triploidy refers to a condition where an individual has 1.5 times the normal number of chromosomes. Egg and sperm cells are haploid (have n number of chromosomes). Normal cells are diploid (have 2n number of chromosomes). The exact cause of triploidy in humans is not known. It may be caused when more than one sperm fertilize a single egg. Triploidy may be preferred and cultivated in plants in order to increase productivity.
That happens in Ana phase.When a chromosome is not split in centromere,a chromosome fully moves to a daughter cell.
Chromosome mutations can result in changes in the number of chromosomes in a cell or changes in the structure of a chromosome. Unlike a gene mutation which alters a single gene or larger segment of DNA on a chromosome, chromosome mutations change and impact the entire chromosome.
The chromosome number at the end of meiosis is half of the parent cell
Homologous chromosomes are separated.
Humans have 46 individual chromosomes. Which translate into 23 pairs.Â
Do you mean Heteroploidy...it is a medical term, an individual or cell possessing a chromosome number other than the normal diploid number
You'd be a multicellular diploid adult (2n=46)
You need the second step to further divide the chromosome into two halves. When that happens the sex cells will have half the chromosomes and when combined with the other sex cell that will produce an individual with one half from the father and one half from the mother.
The modal chromosome number is the most common chromosome number within a population or sample.
I dont think theres a certain number between them both
The chromosome number in hapliod cell is 1 while the dipliod chromosome has 2