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All you need to know about
Prenatal Paternity DNA Testing

















Noninvasive prenatal testing

Not earlier, professionals devised a technology to help ladies of their pregnancy by knowing the paternity before they give birth. To date, Prenatal Paternity DNA Testing assessment is now readily available starting five weeks of pregnancy.

The prenatal paternity testing is carried out accurately using numerous methods. Options include amniocentesis, chorionic villus sampling and fetal genetic substance tests in the course of the 5 to thirteen weeks of pregnancy.

Amniocentesis is a sort of paternity DNA screening that may be invasive. The majority of the time, this is carried out from the later stages of pregnancy. To perform this method, obstetrician trans-abdominally withdraws a small amount of amniotic fluid. The amniotic fluid getting withdrawn is about 10ml. This can be a fantastic sample for paternity screening mainly because amniotic fluid is as accurate as the checks conducted right after their youngster is born.

Immediately after undergoing amniocentesis, results are often released following three to 5 operating days after specimen collection. Amniocentesis costs just the comparable to all other paternity DNA assessment. Nonetheless, obstetrician might opt to charge additional fees for collecting the sample prenatally.

Chronic villus sampling is another sort of invasive paternity DNA assessment. Unlike amniocentesis, constant villus sampling is generally carried out at first stages of pregnancy. Expectant women under eighth to 13th week of pregnancy can go through this procedure.

In performing chronic villus sampling, a catheter is inserted as a result of the cervix. Then, obstetrician obtains sampling from an adequate amount of fetal chorionic villi. Much in-line with amniocentesis, this action is also as exact as the experiment conducted following their child is born.


For other options, non-invasive Natus noninvasive tests screening called fetal genetic materials diagnostic tests are accessible too. That is in a reaction to the risks to fetus posed by previous mentioned invasive solutions. The technology made use of in fetal genetic substance assessment permits obstetricians to work out the paternity of an unborn youngster through an only maternal blood sample. The engineering separates the necessary fetal cells from the mother's blood circulation. These fetal cells are the sampling utilized in finding out the paternity.

Extraction separating primordial fetal cells from the maternal blood samples starts when the laboratory obtains all samples. Professionals say this action can be done about 5 to 12 weeks of fetal gestation. Additionally, fetal genetic substance testing is cost effective and safer compared to other traditional conventional paternity DNA screening.

Thinking about all choices, several specialists say the safest to know the paternity of their child is by utilizing the umbilical cord blood at the time of child's shipping. Testers can deliver final results following three to five working days.

Ways to collect the sample

Self-made cheek swab
FTA Classic Card
Whole Blood
Our Kit
Blood stains
Sperm (Semen)
Fingernail Clippings
Amniotic Fluid
Chorionic Villus Sampling
Fetal Tissue
Chewed Chewing Gum
Cingerete Butts



Hard Candy
Used Condom
Semen Stains
Used Tampons
Used Feminine Pads
spit
Plucked Hair
Q-tips with earwax
Snotty Kleenexes
Electric Razor Debris
Urine
Tooth brushes




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