Nondisjunction is the medical term meaning abnormal condition of meiosis. For example, trisomy 21 (Down syndrome) is a nondisjunction.
For information on a) meiosis (medical) and b) examples of rhetorical statements see the related link below.
Meiotic non-disjunction is used to describe abnormal behavior of sex chromosomes during meiosis although the cause may be non-conjunction or failure of pairing rather than failure of separation of chromosomes or chromatids. The child only has one X chromosome. So the mother must be X+X- and the father is just X+Y. So the child is X- , with the X- from the mom and nothing from dad. B. Yes it can. Non-disjunction n-1 gamete fertilized an egg from mom with the mutant X chromosome. She has the mutant allele from her mother and the non-disjunction came from her father because of the n-1 rule. C. You cannot distinguish whether the abnormal chromosome behavior occurred at the first or second division of meiosis. The reason for this is because with non-disjunction meiosis both parts give you the n-1 rule. So, you cannot tell if it occurred during meiosis I or meiosis II.
If you mean meiosis I and meiosis II, then no they are not identical, but meiosis II does follow meiosis I.
Meiosis
Meiosis I and Meiosis II.
The condition that is caused is a trisomy or a monosomy
For information on a) meiosis (medical) and b) examples of rhetorical statements see the related link below.
Meiotic non-disjunction is used to describe abnormal behavior of sex chromosomes during meiosis although the cause may be non-conjunction or failure of pairing rather than failure of separation of chromosomes or chromatids. The child only has one X chromosome. So the mother must be X+X- and the father is just X+Y. So the child is X- , with the X- from the mom and nothing from dad. B. Yes it can. Non-disjunction n-1 gamete fertilized an egg from mom with the mutant X chromosome. She has the mutant allele from her mother and the non-disjunction came from her father because of the n-1 rule. C. You cannot distinguish whether the abnormal chromosome behavior occurred at the first or second division of meiosis. The reason for this is because with non-disjunction meiosis both parts give you the n-1 rule. So, you cannot tell if it occurred during meiosis I or meiosis II.
Meiosis results in haploid gametes, sperm and egg cells. When the sperm fertilizes the egg, the resulting cell will be diploid, which is the condition of normal body cells.
Mitosis and meiosis are the proper terms for cell division.
Amitosis, meiosis
Meiosis I and meiosis II
meiosis occurs in the overies and the testies.....there is 2 stage of meiosis...meiosis 1 and meiosis
if nondisjunction occurs in meiosis 1 then the resultant sperms are XY carrying sperm n sperm without sex chromosome............ if XY carrying sperm fertilizes with normal X carrying ovum it results in XXY abnormal zygote if sperm without sex chromosome fertilizes with normal X carrying ovum it results in XO abnormal zygote
If you mean meiosis I and meiosis II, then no they are not identical, but meiosis II does follow meiosis I.
Meiosis
The process of meiosis results in gametes (sperm and eggs) which contain one half of the chromosomes (genetic material) of the parent cell. So it results in a reduction of the number of chromosomes. Another term for meiosis is "reduction division".