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BAYLOR GENETICS 2450 HOLCOMBE BLVD. GRAND BLVD. RECEIVING DOCK HOUSTON, TX 770212024PHONE 1.800.411.4363 FAX 1.800.434.9850CONNECTPRENATAL COMPREHENSIVE REQUISITION PATIENT INFORMATION (COMPLETE ONE
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How to fill out prenatal trio whole exome

01
Obtain a blood sample from the pregnant mother
02
Obtain a blood sample from the father
03
Obtain a blood sample from the fetus (usually through amniocentesis or chorionic villus sampling)
04
Extract DNA from the blood samples
05
Sequence the DNA using whole exome sequencing technology
06
Analyze the data to identify any genetic variations or mutations

Who needs prenatal trio whole exome?

01
Prenatal trio whole exome is typically recommended for pregnant women who have a family history of genetic disorders or are at increased risk for having a child with a genetic condition. It may also be recommended for couples who have previously had a child with a genetic disorder or have had recurrent pregnancy losses.
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Prenatal trio whole exome is a genetic test that analyzes the exome of the fetus, mother, and father to identify any potential genetic abnormalities.
Prenatal trio whole exome is usually ordered by healthcare providers for pregnant women who are at higher risk of having a child with a genetic disorder.
Prenatal trio whole exome is typically performed by collecting blood samples from the mother, father, and fetus and sending them to a specialized laboratory for analysis.
The purpose of prenatal trio whole exome is to identify any potential genetic abnormalities in the fetus that may impact its health or development.
The report from prenatal trio whole exome usually includes information about any genetic variants found in the exome of the fetus, mother, and father.
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