Title: Exome Sequencing Identifies a recessive PIGN splice site mutation as a cause of Syndromic Congenital Diaphragmatic Hernia
Authors: Brady, Paul
Van Houdt, Jeroen
Moerman, Philippe
De Catte, Luc
Deprest, Jan
Devriendt, Koenraad
Issue Date: Feb-2014
Host Document: Abstract book pages:107-107
Conference: 14th Annual BeSHG Meeting “Translational Genetics: from cage over bench to bed” location:Antwerp, Belgium date:7 February 2014
Article number: P50
Publication status: published
KU Leuven publication type: AMa
Appears in Collections:Department of Human Genetics - miscellaneous
Laboratory for Cytogenetics and Genome Research
Translational Cell & Tissue Research
Organ Systems (+)

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