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Uncovering recurrent microdeletion syndromes and subtelomeric deletions/duplications through non-selective application of a MLPA-based extended prenatal panel in routine prenatal diagnosis
Authors:Konialis Christopher  Hagnefelt Birgitta  Sevastidou Sophia  Karapanou Sophia  Pispili Katerina  Markaki Aggeliki  Pangalos Constantinos
Affiliation:InterGenetics - Diagnostic Genetics Centre, Athens, Greece. genetic@ath.forthnet.gr
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