Publication | Closed Access
A false positive newborn screening result due to a complex allele carrying two frequent CF-causing variants
15
Citations
13
References
2016
Year
Allelic VariantNeonatal GenomicsNewborn ScreeningFalse Positive NewbornFrequent Cf-causing VariantsGenetic DisorderGeneticsMendelian DisorderGenetic EpidemiologyPediatricsDiagnosisMedicineCarrier ScreeningComplex AlleleVariant Interpretation
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