During meiosis I of a primary spermatocyte (an immature sperm cell that hasn't gone through either round of meiosis yet), the homologous chromosomes are supposed to separate, so the XX and YY chromosomes should separate into two different secondary spermatocytes (I wrote XX and YY since there are two sister chromatids for each chromosome). If non-disjunction occurs here, you'd get an one secondary spermatocyte with XXYY and one with no sex chromosomes (so, that's the answer to your question).
During meiosis II, this sister chromatids separate (i.e. XX separates so that one X is given to each cell, and so on with the rest of the chromosomes). In the XXYY spermatocyte, one copy of X and one copy of Y go to each daughter cell as the sister chromatids separate. This results in two XY spermatids and two spermatids with no sex chromosomes being produced (as long as there isn't another non-disjunction). Then they eventually becoming a mature sperm.
If one of those XY sperm ever makes its way to an egg and fertilizes it, you'd get an XXY zygote (which would usually be viable and always male).
If one of the sex-chromosome-less sperm fertilizes an egg, the zygote would be X0 (female), but probably wouldn't be viable and die in utero.
During meiosis I of a primary spermatocyte (an immature sperm cell that hasn't gone through either round of meiosis yet), the homologous chromosomes are supposed to separate, so the XX and YY chromosomes should separate into two different secondary spermatocytes (I wrote XX and YY since there are two sister chromatids for each chromosome). If non-disjunction occurs here, you'd get an one secondary spermatocyte with XXYY and one with no sex chromosomes (so, that's the answer to your question).
During meiosis II, this sister chromatids separate (i.e. XX separates so that one X is given to each cell, and so on with the rest of the chromosomes). In the XXYY spermatocyte, one copy of X and one copy of Y go to each daughter cell as the sister chromatids separate. This results in two XY spermatids and two spermatids with no sex chromosomes being produced (as long as there isn't another non-disjunction). Then they eventually becoming a mature sperm.
If one of those XY sperm ever makes its way to an egg and fertilizes it, you'd get an XXY zygote (which would usually be viable and always male).
If one of the sex-chromosome-less sperm fertilizes an egg, the zygote would be X0 (female), but probably wouldn't be viable and die in utero.
During meiosis I of a primary spermatocyte (an immature sperm cell that hasn't gone through either round of meiosis yet), the homologous chromosomes are supposed to separate, so the XX and YY chromosomes should separate into two different secondary spermatocytes (I wrote XX and YY since there are two sister chromatids for each chromosome). If non-disjunction occurs here, you'd get an one secondary spermatocyte with XXYY and one with no sex chromosomes (so, that's the answer to your question).
During meiosis II, this sister chromatids separate (i.e. XX separates so that one X is given to each cell, and so on with the rest of the chromosomes). In the XXYY spermatocyte, one copy of X and one copy of Y go to each daughter cell as the sister chromatids separate. This results in two XY spermatids and two spermatids with no sex chromosomes being produced (as long as there isn't another non-disjunction). Then they eventually becoming a mature sperm.
If one of those XY sperm ever makes its way to an egg and fertilizes it, you'd get an XXY zygote (which would usually be viable and always male).
If one of the sex-chromosome-less sperm fertilizes an egg, the zygote would be X0 (female), but probably wouldn't be viable and die in utero.
neither
homologous chromosomes fail to separate during meiosis
Nondisjunction
It is the failure of chromosome pairs to separate properly during cell division.
Nondisjunction is the disappointment of homologous chromosomes to detach accurately during meiosis. This outcomes in the creation of gametes containing a more noteworthy or lesser chromosomal sum than typical ones. Therefore the individual might create a trisomal or monosomal condition.
Nondisjunction
homologous chromosomes fail to separate during meiosis
Nondisjunction
Nondisjunction occurs in too many cells or too few cells causing defects
nondisjunction
Mistakes such as nondisjunction can occur during meiosis. This is the result of chromosomes failing to separate equally during either anaphase.
Nondisjunction is the failure of homologous chromosomes or chromatids to segregate during mitosis or meisos with the result that one daughter cell has both of a pair of parental chromosomes or chromatids and the other has none. An example is Trisomy 21, which is also called Down's Syndrome. This person has 3 chromosome #21.Nondisjunction of genes occur during meiosis I when homologous chromosomes fail to separate or during meiosis II when there is unequal distribution of chromosomes. This leads to aneuploidy.
Nondisjunction, or sending both chromosomes to one cell during meiosis.
yes . it is . nondisjunction is takes place during meiosis.
It is the failure of chromosome pairs to separate properly during cell division.
chromosomes fail to separate during cell division
non disjunction of sex chromosomes
Its called disconjunction. Sometimes it is so bad that they have a miscarriage or the following happens:Trisomy (extra chromosomeso have 47 chromosomes instead of 46)Down's syndrome (andextra number 21 chromosome)Klinefelter's syndrome (males with an extra X chromosome...XXY)