1. A case of the orocraniodigital (Juberg-Hayward) syndrome. Issue 6 (December 1981) Authors: Nevin, N C; Henry, P; Thomas, P T Journal: Journal of medical genetics Issue: Volume 18:Issue 6(1981) Page Start: 478 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A child with a ring G chromosome (46, XX, Gr). Issue 2 (June 1971) Authors: Nevin, N C; MacLaverty, B; Campbell, W A Journal: Journal of medical genetics Issue: Volume 8:Issue 2(1971) Page Start: 231 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A family study of spina bifida and anencephalus in Belfast, Northern Ireland (1964 to 1968). Issue 3 (June 1980) Authors: Nevin, N C; Johnston, W P Journal: Journal of medical genetics Issue: Volume 17:Issue 3(1980) Page Start: 203 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Aglossia-adactylia syndrome. Issue 1 (March 1975) Authors: Nevin, N C; Burrows, D; Allen, G; Kernohan, D C Journal: Journal of medical genetics Issue: Volume 12:Issue 1(1975) Page Start: 89 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalis. Issue 11 (November 1996) Authors: Irvine, A D; Dolan, O M; Hadden, D R; Stewart, F J; Bingham, E A; Nevin, N C Journal: Journal of medical genetics Issue: Volume 33:Issue 11(1996) Page Start: 972 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Anonychia and absence/hypoplasia of distal phalanges (Cooks syndrome): report of a second family. Issue 8 (August 1995) Authors: Nevin, N C; Thomas, P S; Eedy, D J; Shepherd, C Journal: Journal of medical genetics Issue: Volume 32:Issue 8(1995) Page Start: 638 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Antenatal detection of grossly distended bladder owing to absence of the urethra in a fetus with trisomy 18. Issue 2 (April 1983) Authors: Nevin, N C; Nevin, J; Dunlop, J M; Gray, M Journal: Journal of medical genetics Issue: Volume 20:Issue 2(1983) Page Start: 132 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Apparent prevention of neural tube defects by periconceptional vitamin supplementation. Issue 12 (December 1981) Authors: Smithells, R W; Sheppard, S; Schorah, C J; Seller, M J; Nevin, N C; Harris, R; Read, A P; Fielding, D W Journal: Archives of disease in childhood Issue: Volume 56:Issue 12(1981) Page Start: 911 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Carrier estimations in Duchenne muscular dystrophy families in Northern Ireland using RFLP analysis. Issue 2 (February 1990) Authors: Kelly, E D; Graham, C A; Hill, A J; Nevin, N C Journal: Journal of medical genetics Issue: Volume 27:Issue 2(1990) Page Start: 101 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Clinicopathological study of Refsum's disease with particular reference to fatal complications. Issue 4 (April 1978) Authors: Allen, I V; Swallow, M; Nevin, N C; McCormick, D Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 41:Issue 4(1978) Page Start: 323 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗