Publication | Open Access
Noninvasive Prenatal Diagnosis of Single-Gene Disorders by Use of Droplet Digital PCR
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Citations
28
References
2017
Year
Our method detects single-nucleotide mutations of autosomal recessive diseases as early as the first trimester of pregnancy. This is of importance for metabolic disorders in which early diagnosis can affect management of the disease and reduce complications and anxiety related to invasive testing.
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