1. A school based study of children with learning disability indicates poor levels of genetic investigation. Issue 4 (1st April 2002) Authors: FitzPatrick, D R; Pearson, P; Halpin, S; Jackson, P Journal: Journal of medical genetics Issue: Volume 39:Issue 4(2002) Page Start: e19 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Beckwith-Wiedemann syndrome in a child with chromosome 18q deletion. Issue 2 (February 1998) Authors: Brewer, C M; Lam, W W; Hayward, C; Grace, E; Maher, E R; FitzPatrick, D R Journal: Journal of medical genetics Issue: Volume 35:Issue 2(1998) Page Start: 162 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Chromosome analysis: what and when to request. Issue 12 (21st November 2005) Authors: Sharkey, F H; Maher, E; FitzPatrick, D R Journal: Archives of disease in childhood Issue: Volume 90:Issue 12(2005) Page Start: 1264 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Creation and evaluation of full-text literature-derived, feature-weighted disease models of genetically determined developmental disorders. (7th June 2022) Authors: Yates, T.M; Lain, A; Campbell, J; FitzPatrick, D R; Simpson, T I Journal: Database Issue: Volume 2022(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Facial clefts in the west of Scotland in the period 1980-1984: epidemiology and genetic diagnoses. Issue 2 (February 1994) Authors: FitzPatrick, D R; Raine, P A; Boorman, J G Journal: Journal of medical genetics Issue: Volume 31:Issue 2(1994) Page Start: 126 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genetic aspects of admissions to a paediatric intensive care unit. Issue 5 (May 1991) Authors: FitzPatrick, D R; Skeoch, C H; Tolmie, J L Journal: Archives of disease in childhood Issue: Volume 66:Issue 5(1991) Page Start: 639 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Iris coloboma and a microdeletion of chromosome 22: del(22)(q11.22). Issue 11 (1st November 2002) Authors: Morrison, D A; FitzPatrick, D R; Fleck, B W Journal: British journal of ophthalmology Issue: Volume 86:Issue 11(2002) Page Start: 1316 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Neurogenic chronic idiopathic intestinal pseudo-obstruction, patent ductus arteriosus, and thrombocytopenia segregating as an X linked recessive disorder. Issue 8 (August 1997) Authors: FitzPatrick, D R; Strain, L; Thomas, A E; Barr, D G; Todd, A; Smith, N M; Scobie, W G Journal: Journal of medical genetics Issue: Volume 34:Issue 8(1997) Page Start: 666 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Survival in trisomy 13 and trisomy 18 cases ascertained from population based registers. Issue 9 (1st September 2002) Authors: Brewer, C M; Holloway, S H; Stone, D H; Carothers, A D; FitzPatrick, D R Journal: Journal of medical genetics Issue: Volume 39:Issue 9(2002) Page Start: e54 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Zellweger syndrome and associated phenotypes. Issue 10 (October 1996) Authors: FitzPatrick, D R Journal: Journal of medical genetics Issue: Volume 33:Issue 10(1996) Page Start: 863 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗