Yes! A recent example could be babies that do not survive child birth for a certain reason, are obviously unable to pass on whatever caused them to die in the first place.
Also, once humans started to domesticate cows and drink their milk (I'm not sure why humans drink a cow's milk) their bodies evolved to continue making the enzyme to digest milk even after they were weaned off their mothers milk. Many people of Asian descend do not have this enzyme, since their culture did/does not raise as much dairy product.
The number 45 means that the subject has 44 normal autosomal chromosomes (22 chromosomes pairs) plus one (1) good sex chromosome (out of the normal homologous pair). The X0 means that the subject, usually a female, lacks one sister chromosome of the homologous X chromosome pair, or has a partial X sister chromosome.
A carrier of a genetic disorder who does not show symptoms is most likely to be heterozygous for the trait and able to transmit it to offspring. This particular individual has inherited a recessive allele for a genetic trait or mutation but does not display that trait or show symptoms of the disease. They are referred to as genetic carriers. The chance of two carriers having an offspring with the disease or genetic disorder is 25%
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