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There is no way to answer that with out knowing the dominate and recessive traits of both the mother and the father and doing some very long punnett squares with the phenotypes for each. Even after doing that, everything is left up to chance. The punnett squares only offer the percentage or odds of a child having ONE particular trait or another so there is no definite answer.

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Can a child and alleged father have no common DNA markers?

It is extremely rare for a biological father and child to have no shared DNA markers. While small variations can occur due to mutations, genetic testing typically identifies common markers between a father and child. If there are no common DNA markers, it suggests that the alleged father is not the biological parent.


How is the placenta formed in a pregnancy, and how does it incorporate genetic material from the father to support the development of the baby?

During pregnancy, the placenta is formed from cells of both the mother and the embryo. The placenta incorporates genetic material from the father through the embryo's cells, which contain genetic information from both parents. This allows the placenta to provide essential nutrients and oxygen to support the development of the baby throughout pregnancy.


What is the part of a sperm that carries genetic information?

The genetic information in a sperm is carried within the nucleus, which contains the DNA. The sperm's genetic material is tightly packed within the nucleus to ensure it is protected during fertilization.


What statement best describes the genetic information associated with the two of a chromosome?

Each pair of chromosomes contains one chromosome from the mother and one from the father. These two chromosomes carry genetic information that determines an individual's traits and characteristics. The combination of genetic information from both parents contributes to the unique genetic makeup of an individual.


In genetics what if father is also the grandfather?

If the father is also the grandfather, it means that there has been inbreeding within the family. This can lead to an increased risk of genetic disorders or abnormalities in the offspring due to a higher likelihood of inheriting the same harmful genetic mutations from both parents. Inbreeding can also reduce genetic diversity, making it more difficult for the offspring to adapt to changing environments.

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