Colorectal cancer is the third most commonly diagnosed cancer in the United States for men and women. In recent years, new advances in the early detection and treatment of colorectal cancer (also known as colon cancer) suggest a promising future for people with colorectal cancer.

Cell-free DNA screening is known as a non-invasive prenatal screening method with no risk of miscarriage, with a high disease detection rate and low false positive and false negative rates compared to traditional serum screening methods.

Screening for Klinefelter syndrome by invasive diagnostics, requiring amniocentesis or chorionic villus sampling, carries a high risk of miscarriage and fetal malformations. NIPT fetal DNA testing in maternal blood is a new, safe diagnostic method and an effective prenatal screening option for Klinefelter syndrome.

Prenatal screening is one of the important factors that helps pregnant women grasp the health status of the fetus and helps doctors make decisions about intervention before or after birth if the baby has abnormalities.

Prenatal DNA testing to determine whether a man is the father of a fetus before birth. From the 14th week of pregnancy, the mother can test by amniocentesis or prenatal blood testing.

DNA testing samples are very diverse and have similar accuracy such as: blood samples, cells from the oral mucosa, tissue samples, fingernails, hair roots, umbilical cords, bones, teeth,...

Fingerprints have been used for over 2000 years. They have been extensively studied by anthropologists and biologists. A person's fingerprints begin to form around the 13th week of pregnancy and are completed around the 19th to 24th week. Fingerprints are unique, difficult to change, and remain relatively stable throughout a person's life. They represent a person's basic characteristics.

DNA fingerprints can be used to determine blood relationships, track down criminals through biological traces containing DNA left at the scene, or track down victims through living bodies, even if they are just bone fragments or teeth. This is a great advancement in forensic science.

Genetic testing results can confirm or rule out a genetic disease, help determine a person's risk of developing or passing on a genetic disorder to future generations, and determine a person's DNA.

When you are pregnant, you may receive a lot of unwanted comments about your body and your baby. One of the most common topics of discussion is whether you are carrying a boy or a girl. There are many old wives’ tales and other folklore about this issue. Here are some facts to help you separate myth from fact.

Muscular dystrophy is a genetic disease. Although it is not common, the possibility of passing it on to the next generation is quite high. How to treat muscular dystrophy is still a question for the scientific community. However, some current medical achievements are still being applied to diagnose and treat muscular dystrophy.