Go to the Doctor
Chat with our AI personalities
To determine if a child has an extra half of a chromosome, genetic testing such as a chromosomal microarray analysis or a karyotype test would be needed. These tests can identify any abnormalities in the number or structure of chromosomes in an individual's cells. It is important to consult with a healthcare professional or a genetic counselor for proper diagnosis and guidance.
If you are female, you receive half of your father's genetic material. If you are male, you receive almost half; the Y chromosome is missing some genes, so it is the mother's X chromosome and the genes on the top of it that solely determine certain characteristics in the son. These are called sex-linked characteristics.
The gene for this trait is likely located on the Y chromosome. The Y chromosome is passed down from father to son, and since only males have a Y chromosome, the trait will only be passed down through male lineage.
yes, some people have xxy chromosomes, a genetic mutation. Although I'm not sure if the extra chromosome is from the fathers sperm or sex cell. Hope this helps :)
Y-linked genes are only passed from father to son because the Y chromosome is inherited exclusively in a paternal manner. Since females inherit an X chromosome from each parent, they do not receive a Y chromosome from their father.
If the mother is a carrier for hemophilia, there is a 50% chance that her sons will inherit the hemophilia gene, but only if the father does not have hemophilia. This is because sons inherit the X chromosome that carries the hemophilia gene from their mother. If the father does not have hemophilia, the son will not inherit a healthy X chromosome from him to compensate for the defective X chromosome from the mother.