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. 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) ↗
4. Service experience using DNA analysis for genetic prediction in Duchenne muscular dystrophy. Issue 1 (January 1988) Authors: Goodship, J; Malcolm, S; Robertson, M E; Pembrey, M E Journal: Journal of medical genetics Issue: Volume 25:Issue 1(1988) Page Start: 14 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Role of genetic variation in the transcriptional inhibitor protein Smad6 in the predisposition to congenital cardiovascular malformation. (22nd September 2015) Authors: Tan, HL; Topf, A; Griffin, H; Palomino Doza, J; Hall, D; Hussain, R; Eden, J; Rahman, T; Cunnington, M; Goodship, J; Keavney, B Journal: Heart Issue: Volume 95(2009)Supplement 1 Page Start: 101 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Monozygotic twins with chromosome 22q11 deletion and discordant phenotype. Issue 9 (September 1995) Authors: Goodship, J; Cross, I; Scambler, P; Burn, J Journal: Journal of medical genetics Issue: Volume 32:Issue 9(1995) Page Start: 746 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Transmission of Proteus syndrome from father to son?. Issue 11 (November 1991) Authors: Goodship, J; Redfearn, A; Milligan, D; Gardner-Medwin, D; Burn, J Journal: Journal of medical genetics Issue: Volume 28:Issue 11(1991) Page Start: 781 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasia. Issue 7 (July 1990) Authors: Goodship, J; Malcolm, S; Clarke, A; Pembrey, M E Journal: Journal of medical genetics Issue: Volume 27:Issue 7(1990) Page Start: 422 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. 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) ↗
10. 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) ↗