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Screening of 22q11.2DS Using Multiplex Ligation-Dependent Probe Amplification as an Alternative Diagnostic Method.

Sathiya MaranSiti Aisyah FatenSwee-Hua Erin LimKok-Song LaiWan Pauzi Wan IbrahimRavindran AnkathilSiew Hua GanHuay Lin Tan
Published in: BioMed research international (2020)
The incidence of 22q11.2DS among patients with CHD in the east coast of Malaysia is 0.047. MLPA is a scalable and affordable alternative molecular diagnostic method in the screening of 22q11.2DS and can be routinely applied for the diagnosis of deletion syndromes.
Keyphrases
  • risk factors
  • high throughput
  • living cells