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That it is a BOY, male infant

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15y ago

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Should the government pay for genetic testing?

The federal government should pay for medical genetic testing if it will help advance society towards controlling or eliminating deadly diseases or disorders. A criteria should be set up to determine what test should be approved for financing.


Are dimples from a mutation on the chromosomes?

dimples are a "birth defect" means that your muscles are too short thus pulling the skin causing this little holes, why do you think most babies have them? cause their muscles developed and they have a lot of baby fat same goes to people with a little extra fat


What is gene cloning and gene modification?

Gene cloning is when you take the entire genetic profile to create a copy of the donor of the genes. Gene modification is when you change a persons genes, in a way to change the outcome of how the baby will look, act, her/his personality and a lot more. In this case, gene cloning would come under the category of gene manipulation.


Can a baby from two lesbian parents have both genes in the baby so they can look like both parents?

This is a rather difficult question to answer. In theory it's possible. A baby requires X and Y chromosomes. The Y chromosome is only found in males. While it is possible to genetically engineer babies, they still need male genetic interaction. In theory it may be possible to genetically engineer the baby from one egg and sperm, then have the other partners genes engineered into the baby during growth in the womb. You can't make a baby without sperm. While in theory the above is possible, it has not been scientifically proven as successful. The process I have described above is called artificial parthenogenesis. The method has been tested on insects and rats in a lab, both with varying levels of success and failure. So far, unfortunately there has been no success with humans, but scientists are still researching, because they have managed to make it work in rats and insects. The problem is that human DNA is the most complex DNA structure on Earth. Even if an experiment is successful the resulting child would be under scientific observation for his/her life to ensure the process doesn't cause health issues, before the procedure is available to the public. You should also bear in mind that genetic engineering is extremely controversial. One single slip-up during engineering will change the future of humankind. One other thing you could try, is to have your parter donate her egg to you and have that egg fertilised by a sperm in your womb. I advise you to speak to a fertility or family planning doctor about this, you never know what you might learn. Wish you the best of luck.


If a miscarriage is most often the result of chromosonal abnormalities would it be wise to have genetic testing done the next time you become pregnant?

Many women miscarry, as many as one in four, but it is usually a one off and they will go on to have a healthy baby. Providing you don't keep miscarrying (and there are many reasons for this beside a chromosomal abnormality) don't worry about it. If you do repeatedly miscarry you may be referred for genetic testing, but that is just one of the tests which will be done.

Related Questions

What naturally occurring chemical must be present for you to have a baby boy?

Male sperm determine the sex of the baby, not chemicals, etc.


Is the baby guaranteed to be free from genetic disorders if the chromosome configuration appears normal?

If you are pregnant there are many thoughts running through your mind including the potential health of your unborn baby. There is no guarantee the baby will be free if the genetic testing comes back clear, however, there is a good chance all will be well. If you have any concerns, talk to your doctor.


What is a chromosome cell and how does it work?

A chromosome cell's ie. The egg and sperm cell carry genetic information in the form of chromosomes 23 from the mother and farther so 46 in total these are the starting point of DNA. This determines how the baby will look like and its physical capability's will be.


How is a baby sexs determine?

It's determined by the genetic chromosome of the sperm. Women have only one X chromosome in the egg (both egg and sperm have 23 pairs of chromosomes, which unite to form 46). On the other hand, men have either X or Y chromosomes. If an egg (X chromosome) joins with an X chromosome sperm, the result will be a girl. If an egg (X chromosome) joins with a Y chromosome sperm, the result will be a boy. In other words: the guy determines the sex of a baby :)


Who makes the sex of the baby?

The chromosome in the male's gamete determines the gender of the baby. If it is a Y chromosome, the baby will be a boy. If the chromosome is a X, the baby will be a girl.


What does the nucleus inside the head of the sperm do?

It carries genetic information.It gives paternal genetic information to baby.


When is the sex of baby decided?

The sex of a baby is determined at conception when the sperm fertilizes the egg. Each sperm carries either an X or Y chromosome, while the egg carries an X chromosome. If the sperm carries an X chromosome, the resulting embryo will be female (XX), while a Y chromosome from the sperm will lead to a male embryo (XY). This genetic determination occurs before the embryo implants in the uterus.


What is a disadvantage of analysing chromosome number and the genetic sequences in the amniotic fluid allowing the doctor to diagnose the gender of the baby as well as any genetic disease in the baby?

Because the parents might choose to abort a baby that isn't of the preferred gender (if the parents wanted a boy they might abort a fetus that is a girl).


How do X and Y chromosome differ?

The X chromosome is larger and carries more genetic information than the Y chromosome. The Y chromosome carries the genes that determine male sex characteristics, while the X chromosome carries genes that are important for both male and female development. Males typically have one X and one Y chromosome, while females have two X chromosomes.


Sex determination in the unborn baby?

Sex determination in an unborn baby is determined by the combination of sex chromosomes inherited from the parents. Typically, females have two X chromosomes (XX) and males have one X and one Y chromosome (XY). During fertilization, the father's sperm can contribute either an X or a Y chromosome, determining the genetic sex of the offspring. This process occurs at the moment of conception and is responsible for the development of the baby's sex characteristics.


What gender would a baby be if it had an x chromosome and a y chromosome?

boy


What gender would a baby be if it had a X chromosome and a Y chromosome?

boy