1. Angelman's syndrome and 15q11-13 deletions. Issue 8 (August 1989) Authors: Fryns, J P; Kleczkowska, A; Decock, P; Van den Berghe, H Journal: Journal of medical genetics Issue: Volume 26:Issue 8(1989) Page Start: 538 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Auralcephalosyndactyly: a new craniosynostosis syndrome or a variant of the Saethre-Chotzen syndrome?. Issue 8 (August 1989) Authors: Legius, E; Fryns, J P; Van den Berghe, H Journal: Journal of medical genetics Issue: Volume 26:Issue 8(1989) Page Start: 522 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Congenital leukaemia with 46, XX, t(Bq+, Cq-) cells. Issue 4 (December 1972) Authors: Van den Berghe, H; Fryns, J P; Verresen, H Journal: Journal of medical genetics Issue: Volume 9:Issue 4(1972) Page Start: 468 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. EEC syndrome without ectrodactyly: report of two new families. Issue 3 (March 1990) Authors: Fryns, J P; Legius, E; Dereymaeker, A M; Van den Berghe, H Journal: Journal of medical genetics Issue: Volume 27:Issue 3(1990) Page Start: 165 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Familial transmission of autosomal whole arm translocation. Issue 11 (November 1988) Authors: Fryns, J P; Kleczkowska, A; Van den Berghe, H Journal: Journal of medical genetics Issue: Volume 25:Issue 11(1988) Page Start: 783 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Hypohidrotic ectodermal dysplasia, primary hypothyroidism, and agenesis of the corpus callosum. Issue 8 (August 1989) Authors: Fryns, J P; Chrzanowska, K; Van den Berghe, H Journal: Journal of medical genetics Issue: Volume 26:Issue 8(1989) Page Start: 520 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Is the expression of fra(2)(q13) age dependent?. Issue 10 (October 1988) Authors: Fryns, J P; Van den Berghe, H Journal: Journal of medical genetics Issue: Volume 25:Issue 10(1988) Page Start: 718 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Perception of predictive testing for Huntington's disease by young women: preferring uncertainty to certainty?. Issue 7 (July 1993) Authors: Decruyenaere, M; Evers-Kiebooms, G; Van den Berghe, H Journal: Journal of medical genetics Issue: Volume 30:Issue 7(1993) Page Start: 557 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Prediction of psychological functioning one year after the predictive test for Huntington's disease and impact of the test result on reproductive decision making. Issue 9 (September 1996) Authors: Decruyenaere, M; Evers-Kiebooms, G; Boogaerts, A; Cassiman, J J; Cloostermans, T; Demyttenaere, K; Dom, R; Fryns, J P; Van den Berghe, H Journal: Journal of medical genetics Issue: Volume 33:Issue 9(1996) Page Start: 737 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Profound mental retardation, characteristic facies with midfacial hypoplasia and premature frontotemporal balding, muscular hypotrophy, and small patellae in two unrelated male patients. Issue 4 (April 1993) Authors: Fryns, J P; Thiry, P; Geutjens, J; Smeets, E; Vinken, L; Van den Berghe, H Journal: Journal of medical genetics Issue: Volume 30:Issue 4(1993) Page Start: 319 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗