Next generation sequencing of SNPs for non-invasive prenatal diagnosis: challenges and feasibility as illustrated by an application to β-thalassaemia
Thessalia Papasavva(Cyprus Institute of Neurology and Genetics), Marina Kleanthous(Cyprus Institute of Neurology and Genetics), Loukas Kythreotis(Archbishop Makarios III Hospital), Christel Kockx(Erasmus University Rotterdam), Frank Grosveld(Erasmus MC), Eleni Ι. Kalogirou(Archbishop Makarios III Hospital), Wilfred F. J. van IJcken(Erasmus MC), Mirjam C. G. N. van den Hout(Erasmus MC), Petros Kountouris(Cyprus Institute of Neurology and Genetics)
Cited by 55
Related Papers
Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome
|The Journal of Experimental Medicine|2016|289
Novel binding partners of Ldb1 are required for haematopoietic development
|Development|2006|135