Associated Papers
Discovery of rare ancestry-specific variants in the fetal genome that confer risk of preterm premature rupture of membranes (PPROM) and preterm birth.
Modi BP et al.
Bmc Medical Genetics, 2018
Whole exome sequencing identification of novel candidate genes in patients with proliferative diabetic retinopathy.
Ung C et al.
Vision Research, 2017
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