1. Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree. Issue 4 (April 1989) Authors: Suthers, G K; Manson, J I; Stern, L M; Haan, E A; Mulley, J C Journal: Journal of medical genetics Issue: Volume 26:Issue 4(1989) Page Start: 251 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Characterisation of four novel fibrillin-1 (FBN1) mutations in Marfan syndrome. Issue 8 (August 1996) Authors: Adès, L C; Haan, E A; Colley, A F; Richard, R I Journal: Journal of medical genetics Issue: Volume 33:Issue 8(1996) Page Start: 665 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Congenital heart malformation in Yunis-Varón syndrome. Issue 9 (September 1993) Authors: Adès, L C; Morris, L L; Richardson, M; Pearson, C; Haan, E A Journal: Journal of medical genetics Issue: Volume 30:Issue 9(1993) Page Start: 788 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Does sacral agenesis predispose to spina bifida?. Issue 4 (August 1983) Authors: Magnus, R; Rogers, J G; Haan, E A Journal: Journal of medical genetics Issue: Volume 20:Issue 4(1983) Page Start: 313 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Humeroradioulnar synostosis in a patient with lambdoid synostosis. Issue 1 (January 1993) Authors: Edwards, T J; Haan, E A; Humphrey, I J Journal: Journal of medical genetics Issue: Volume 30:Issue 1(1993) Page Start: 81 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Hydrocephalus in Hajdu-Cheney syndrome. Issue 2 (February 1993) Authors: Adès, L C; Morris, L L; Haan, E A Journal: Journal of medical genetics Issue: Volume 30:Issue 2(1993) Page Start: 175 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Origins of accessory small ring marker chromosomes derived from chromosome 1. Issue 11 (1st November 1999) Authors: Callen, D F; Eyre, H; Fang, Y-Y; Guan, X-Y; Veleba, A; Martin, N J; McGill, J; Haan, E A Journal: Journal of medical genetics Issue: Volume 36:Issue 11(1999) Page Start: 847 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Predictive diagnosis of myotonic dystrophy with flanking microsatellite markers. Issue 7 (July 1991) Authors: Mulley, J C; Gedeon, A K; White, S J; Haan, E A; Richards, R I Journal: Journal of medical genetics Issue: Volume 28:Issue 7(1991) Page Start: 448 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Prevalence of neural tube defects in South Australia, 1966-91: effectiveness and impact of prenatal diagnosis. Issue 6906 (18th September 1993) Authors: Chan, A; Robertson, E F; Haan, E A; Keane, R J; Ranieri, E; Carney, A Journal: BMJ Issue: Volume 307:Issue 6906(1993) Page Start: 703 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16. Issue 3 (March 1990) Authors: Callen, D F; Ringenbergs, M L; Fowler, J C; Freemantle, C J; Haan, E A Journal: Journal of medical genetics Issue: Volume 27:Issue 3(1990) Page Start: 155 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗