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FISH for William syndrome (DNA Center)
SKU: MD-NLB392 Categories: , , , , , , , , , , Tags: , , , , , ,

In Stock

FISH for William syndrome (DNA Center)

฿8,463.00

Additional information

Also Known As

Williams Syndrome Test, FISH for Genetic Deletions
Specimen

Heparinized whole blood 5 ml. (Minimun Vol 3 ml.)
Turnaround Time

16 days
Test Code

MD-NLB392
Test Type

Special
Related Tests

Chromosome Study, FISH for Chromosome 7

Detects genetic deletions associated with Williams syndrome using FISH, a genetic test used to confirm the diagnosis in patients with characteristic facial features and developmental delays.

Product tags: Cardiovascular Issues, Developmental Disorders, FISH for Genetic Deletions, Genetic Disorders, Intellectual Disability, None, Williams Syndrome Test
Diseases: Developmental Disorders, Genetic Disorders
Symptoms: Cardiovascular Issues, Intellectual Disability
Habits: None
Age Groups: Adults, Pediatrics
Specimens: Heparinized Whole Blood
Diagnostic Methods: FISH, Fluorescence In Situ Hybridization
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Description

Detects genetic deletions associated with Williams syndrome using FISH, a genetic test used to confirm the diagnosis in patients with characteristic facial features and developmental delays.

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

Williams Syndrome Test, FISH for Genetic Deletions
Specimen

Heparinized whole blood 5 ml. (Minimun Vol 3 ml.)
Turnaround Time

16 days
Test Code

MD-NLB392
Test Type

Special
Related Tests

Chromosome Study, FISH for Chromosome 7

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