Publications by authors named "Maryse De Smedt"

4Publications

2q31.1 microdeletion syndrome: redefining the associated clinical phenotype.

J Med Genet 2011 Feb 10;48(2):98-104. Epub 2010 Nov 10.

Centre for Human Genetics, University Hospitals Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1136/jmg.2010.079491DOI Listing
February 2011

A boy with an unusual association of ventral midline anomalies including a trunk-like umbilicus.

Clin Dysmorphol 2004 Oct;13(4):261-3

Centre for Human Genetics, Division of Clinical Genetics, University Hospital Leuven, Herestraat 49, B-3000 Leuven, Belgium.

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http://dx.doi.org/10.1097/00019605-200410000-00013DOI Listing
October 2004