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Publications by authors named "S Gaillez"

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Diagnostic pitfall in antenatal manifestations of CPT II deficiency.
F Boemer, M Deberg, R Schoos, J-H Caberg, S Gaillez

Clin Genet· February 2016


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Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges.
Olivier Vanakker, Catheline Vilain, Katrien Janssens, Nathalie Van der Aa, Guillaume Smits, Stéphane Gaillez

Eur J Med Genet· March 2014


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Clinical, cytogenetic and molecular characterization of two cases of mosaic ring chromosome 13.
A Uwineza, G Pierquin, S Gaillez, M Jamar, A C Hellin

Genet Couns· October 2013


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[Are we genetically predisposed to addictions?].
E Castermans, S Gaillez, V Bours

Rev Med Liege· August 2013


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Rapid prenatal diagnosis of fetal Zellweger syndrome by biochemical tests, complementation studies, and molecular analyses.
Karin Segers, Genevieve Pierquin, Stephanie Gaillez, Katty Delbecque, Maria Retz

Prenat Diagn· February 2013


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