https://www.selleckchem.com/pr....oducts/gsk1838705a.h
We describe 2 unusual haemoglobin (Hb) Bart's hydrops cases that could not be explained by traditional factors. Two families with a diagnosis or history of foetal hydrops were enrolled. A suspension-array system was used to detect the 23 most frequent mutations in southern China. Multiplex ligation-dependent probe amplification (MLPA) was used to screen for possible deletions. Precise characterisation of the breakpoints of the novel variants and uniparental disomy analysis were performed using a single nucleotide polymorphism (SNP)
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