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Lahalak Medical PlatformDifferentiate Care
Beckwith-Wiedemann Syndrome (H19) Genetic Sequencing
Identify genetic variants associated with Beckwith-Wiedemann Syndrome by sequencing the H19 regulatory region, enabling early diagnosis and the development of a specialized medical care plan for your child.
Advanced genetic test sequencing the H19 regulatory region to detect mutations causing Beckwith-Wiedemann Syndrome, a growth disorder that may increase the risk of certain pediatric tumors.
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