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Prenatal diagnosis for single gene mutation + chromosome study (Genome star)
SKU: MD-NLMA426 Categories: , , , , , , , , , Tags: , , , , ,

In Stock

Prenatal diagnosis for single gene mutation + chromosome study (Genome star)

฿33,600.00

Additional information

Also Known As

Prenatal Genetic Diagnosis
Specimen

Amniotic fluid 20-25 ml and Maternal EDTA blood 3 ml.
Turnaround Time

23 days
Test Code

MD-NLMA426
Test Type

Special
Related Tests

Amniocentesis, Carrier Screening

Diagnoses genetic mutations and chromosomal abnormalities in fetuses using amniotic fluid samples.

Product tags: Family History of Genetic Conditions, Family Planning, Genetic Disorders, Miscarriage, Prenatal Genetic Diagnosis, Prenatal Testing
Diseases: Genetic Disorders, Prenatal Testing
Symptoms: Family History of Genetic Conditions, Miscarriage
Habits: Family Planning
Age Groups: Pregnant Women
Specimens: Amniotic Fluid, Maternal EDTA Blood
Diagnostic Methods: PCR and Karyotyping
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Description

Diagnoses genetic mutations and chromosomal abnormalities in fetuses using amniotic fluid samples.

This lab test includes home sample collection via a provided kit or by a clinician, and you'll receive a comprehensive physical health report with your results.

Additional information

Also Known As

Prenatal Genetic Diagnosis
Specimen

Amniotic fluid 20-25 ml and Maternal EDTA blood 3 ml.
Turnaround Time

23 days
Test Code

MD-NLMA426
Test Type

Special
Related Tests

Amniocentesis, Carrier Screening

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