Yes. It is known as Klinefelter's syndrome. The extra X chromosome interferes with meiosis and usually prevents the affected males from reproducing.
Yes. That chromosome disjunction event is called Kleinfelter's syndrome. PS Sex. Biologists use the word sex.
No. If it is a mother, that infers that the organism is female. The feature that determines gender is the 23rd set of chromosomes. A female can only result if the pair is XX (XY results in a male). Therefore, a mother cannot pass on a Y chromosome to her child. If you are wondering whether by cause of a genetic mutation the mother happens to have a Y chromosome, then she would not be a mother, as she would be infertile.
A haploid Chromosome set. {Or, a haploid set of Chromosomes.}
A superfemale has an extra X chromosome for a sex chromosome set of XXX. The characteristics of a superfemale is that she may have speech and verbal deficiency.
There will be two copies of each chromosome in all somatic cells called homologous chromosome..In case of reproductive cells there will be only one set during gamete formation...
Yes. That chromosome disjunction event is called Kleinfelter's syndrome. PS Sex. Biologists use the word sex.
It is a condition in which human males have an extra X chromosome. It is inherited when the extra X chromosome is retained because of a nondisjunction event during meiosis I (gametogenesis).
a set chromosome define about progeny which could be male or female
There are 2 of each chromosome because you get 1 set from each parent.
No. If it is a mother, that infers that the organism is female. The feature that determines gender is the 23rd set of chromosomes. A female can only result if the pair is XX (XY results in a male). Therefore, a mother cannot pass on a Y chromosome to her child. If you are wondering whether by cause of a genetic mutation the mother happens to have a Y chromosome, then she would not be a mother, as she would be infertile.
If it has a x and y chromosome it is from a male if it has two x chromosome or is from a female
A haploid Chromosome set. {Or, a haploid set of Chromosomes.}
Monosomy occurs when one chromosome is absent from the normal diploid number. This is referred to as aneuploidy which is the loss or gain of a chromosome during meiosis.An example of monosomy is Turner Syndrome. One of the sex chromosomes is missing. In an unaffected female there are 2 'X' chromosomes. But in Turner Syndrome there is one sex chromosome missing.Trisomy occurs when there is three copies of a chromosome instead of the normal diploid number. This is also referred to as aneuploidy because there was an extra chromosome added hence, an abnormal amount of chromosomes.An example of trisomy is in Trisomy 21(Downs Syndrome) in which chromosome 21 has an extra chromosome.
A superfemale has an extra X chromosome for a sex chromosome set of XXX. The characteristics of a superfemale is that she may have speech and verbal deficiency.
There will be two copies of each chromosome in all somatic cells called homologous chromosome..In case of reproductive cells there will be only one set during gamete formation...
Because human gametes are of two kinds, sperm (male) and egg (female). The two come together to make 1 cell called a zygote. That then replicates and creates all your other cells. 23 + 23 = 46. That's why!
An animal will have a full set of chromosomes (2n) as an embryo.