you can get a genetic (it runs in families, so if your immediate relatives have not got it, its a good chance you wont either) disease called Huntington's Disease that affects the genes and chromosome, that causes death because it is a mutation of the genes, but otherwise, i don't know.
DNA or genens these are the segments of the chromosome.
Life man yeah dude
The most well characterized genes include DCX on the X chromosome, responsible for double cortex syndrome, and LIS1 on chromosome 17, the first gene identified for lissencephaly.
Too few of a type of chromosome can cause genetic disorders or death. Turner Syndrome occurs when there is a missing X chromosome.
The element responsible for determining male sex in humans is the Y chromosome.
The pseudoautosomal regions (PARs) at the tips of the Y chromosome are homologous to regions on the X chromosome. These PARs are responsible for pairing and recombination between the X and Y chromosomes during meiosis. About 5% of the Y chromosome is homologous to the X chromosome in humans.
Abel was killed by his brother Cain, who was responsible for his death.
Genes on the Y chromosome are responsible for male sex determination and other male-specific traits. They play a crucial role in the development of male reproductive organs and secondary sexual characteristics.
In humans, the Y chromosome is noticeably shorter than the X chromosome.
Men are responsible for the gender of their children due to the contribution of their sperm, which carries either an X or a Y chromosome. Women contribute an X chromosome through their eggs. If the sperm carrying a Y chromosome fertilizes the egg, the child will be male (XY), while an X chromosome from the sperm results in a female child (XX). Thus, the combination of the chromosomes from both parents determines the child's gender.
The allele that is responsible of Fabry Disorder/Disease is located on the X chromosome and is the only lipid storage disorder identified as being sex linked.
Color blindness is typically inherited in an X-linked recessive pattern. This means that a son inherits his X chromosome from his mother and his Y chromosome from his father. Therefore, regardless of the mother's phenotype, she is the parent responsible for passing on the X chromosome that may carry the gene for color blindness, while the father contributes a Y chromosome. If the mother is a carrier or affected, there is a chance for the son to be color blind.