1. 131 Aetiological role of folate deficiency in congenital heart disease: evidence from Mendelian randomisation and meta-analysis. (9th June 2011) Authors: Mamasoula, V; Pierscionek, T; Hall, D; Palomino-Doza, J; Topf, A; Rahman, T; Goodship, J; Keavney, B Journal: Heart Issue: Volume 97(2011)Supplement 1 Page Start: A75 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 134 Mutations in the sarcomere protein gene MYH7 in Ebstein's anomaly. (9th June 2011) Authors: Rahman, T; Goodship, J; Postma, A; Engelen, K; Mulder, B; Klaassen, S; Keavney, B Journal: Heart Issue: Volume 97(2011)Supplement 1 Page Start: A76 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A male with type I orofaciodigital syndrome. Issue 10 (October 1991) Authors: Goodship, J; Platt, J; Smith, R; Burn, J Journal: Journal of medical genetics Issue: Volume 28:Issue 10(1991) Page Start: 691 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Defects in the determination of left-right asymmetry. Issue 6 (June 1996) Authors: Splitt, M P; Burn, J; Goodship, J Journal: Journal of medical genetics Issue: Volume 33:Issue 6(1996) Page Start: 498 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. DiGeorge syndrome: part of CATCH 22. Issue 10 (October 1993) Authors: Wilson, D I; Burn, J; Scambler, P; Goodship, J Journal: Journal of medical genetics Issue: Volume 30:Issue 10(1993) Page Start: 852 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Floating-Harbor syndrome. Issue 3 (March 1991) Authors: Patton, M A; Hurst, J; Donnai, D; McKeown, C M; Cole, T; Goodship, J Journal: Journal of medical genetics Issue: Volume 28:Issue 3(1991) Page Start: 201 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Intellectual development in Apert's syndrome: a long term follow up of 29 patients. Issue 3 (March 1988) Authors: Patton, M A; Goodship, J; Hayward, R; Lansdown, R Journal: Journal of medical genetics Issue: Volume 25:Issue 3(1988) Page Start: 164 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Investigation into the Importance of genes encoding ciliary proteins in congenital heart disease using whole exome sequencing. Issue 1 (December 2015) Authors: Hartill, V; Logan, C; Parry, DA; Szymanska, K; Ashcroft, K; English, K; Prescott, K; Dobbie, A; Barwick, S; Bennett, C; Goodship, J; Sheridan, E; Johnson, C Journal: Cilia Issue: Volume 4:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134). Issue 10 (October 1993) Authors: Wadey, R; Daw, S; Wickremasinghe, A; Roberts, C; Wilson, D; Goodship, J; Burn, J; Halford, S; Scambler, P J Journal: Journal of medical genetics Issue: Volume 30:Issue 10(1993) Page Start: 818 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency cluster. Issue 12 (December 1998) Authors: Goodship, J Journal: Journal of medical genetics Issue: Volume 35:Issue 12(1998) Page Start: 1054 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗