1. Cardiovascular malformations in DiGeorge syndrome (congenital absence of hypoplasia of the thymus). Issue 4 (October 1980) Authors: Moerman, P; Goddeeris, P; Lauwerijns, J; Van der Hauwaert, L G Journal: Heart Issue: Volume 44:Issue 4(1980) Page Start: 452 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Chromosome 22q11 deletion presenting as the Potter sequence. Issue 5 (May 1997) Authors: Devriendt, K; Moerman, P; Van Schoubroeck, D; Vandenberghe, K; Fryns, J P Journal: Journal of medical genetics Issue: Volume 34:Issue 5(1997) Page Start: 423 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Congenital atresia of left coronary ostium. Issue 3 (September 1982) Authors: van der Hauwaert, L G; Dumoulin, M; Moerman, P Journal: Heart Issue: Volume 48:Issue 3(1982) Page Start: 298 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Early onset asymmetrical intrauterine growth retardation with fetal hypokinesia and variable expression of acral and genitourinary malformations: a new lethal MCA syndrome. Issue 1 (1st January 2003) Authors: Witters, I; Moerman, P; Van Assche, F A; Fryns, J-P Journal: Journal of medical genetics Issue: Volume 40:Issue 1(2003) Page Start: e1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Holoprosencephaly and postaxial polydactyly: another observation. Issue 7 (July 1988) Authors: Moerman, P; Fryns, J P Journal: Journal of medical genetics Issue: Volume 25:Issue 7(1988) Page Start: 501 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Interrupted right aortic arch in DiGeorge syndrome. Issue 3 (September 1987) Authors: Moerman, P; Dumoulin, M; Lauweryns, J; Van der Hauwaert, L G Journal: Heart Issue: Volume 58:Issue 3(1987) Page Start: 274 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Physical and psychomotor development of 1799 children born after second trimester amniocentesis for maternal serum positive triple test screening and normal prenatal karyotype. Issue 12 (1st December 2002) Authors: Witters, I; Moerman, P; Van Assche, A; Fryns, J-P Journal: Journal of medical genetics Issue: Volume 39:Issue 12(2002) Page Start: e75 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Severe primary pulmonary hypoplasia ("acinar dysplasia") in sibs: a genetically determined mesodermal defect?. Issue 11 (November 1998) Authors: Moerman, P; Vanhole, C; Devlieger, H; Fryns, J P Journal: Journal of medical genetics Issue: Volume 35:Issue 11(1998) Page Start: 964 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Short limbed dwarfism, genital hypoplasia, sparse hair, and vertebral anomalies: a variant of Ellis-van Creveld syndrome?. Issue 4 (April 1993) Authors: Fryns, J P; Moerman, P Journal: Journal of medical genetics Issue: Volume 30:Issue 4(1993) Page Start: 322 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Triple negative breast cancer: a study from the point of view of basal CK5/6 and HER-1. Issue 7 (26th June 2009) Authors: Pintens, S; Neven, P; Drijkoningen, M; Van Belle, V; Moerman, P; Christiaens, M-R; Smeets, A; Wildiers, H; Bempt, I Vanden Journal: Journal of clinical pathology Issue: Volume 62:Issue 7(2009) Page Start: 624 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗