1. A rare heteromorphism of chromosome 20 and reproductive loss. Issue 7 (July 1991) Authors: Romain, D R; Whyte, S; Callen, D F; Eyre, H J Journal: Journal of medical genetics Issue: Volume 28:Issue 7(1991) Page Start: 477 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Expression of ZNF652, a novel zinc finger protein, in vulvar carcinomas and its relation to prognosis. Issue 1 (27th April 2007) Authors: Holm, R; Knopp, S; Kumar, R; Lee, J; Nesland, J M; Tropè, C; Callen, D F Journal: Journal of clinical pathology Issue: Volume 61:Issue 1(2008) Page Start: 59 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype. Issue 10 (October 1993) Authors: Callen, D F; Eyre, H; Lane, S; Shen, Y; Hansmann, I; Spinner, N; Zackai, E; McDonald-McGinn, D; Schuffenhauer, S; Wauters, J Journal: Journal of medical genetics Issue: Volume 30:Issue 10(1993) Page Start: 828 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1). Issue 10 (October 1990) Authors: Breuning, M H; Snijdewint, F G; Brunner, H; Verwest, A; Ijdo, J W; Saris, J J; Dauwerse, J G; Blonden, L; Keith, T; Callen, D F Journal: Journal of medical genetics Issue: Volume 27:Issue 10(1990) Page Start: 603 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Mapping the human alpha globin gene complex to 16p13.2----pter. Issue 12 (December 1987) Authors: Simmers, R N; Mulley, J C; Hyland, V J; Callen, D F; Sutherland, G R Journal: Journal of medical genetics Issue: Volume 24:Issue 12(1987) Page Start: 761 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivation. Issue 2 (February 1995) Authors: Callen, D F; Eyre, H J; Dolman, G; Garry-Battersby, M B; McCreanor, J R; Valeba, A; McGill, J J Journal: Journal of medical genetics Issue: Volume 32:Issue 2(1995) Page Start: 113 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Molecular genetics of human chromosome 16. Issue 8 (August 1987) Authors: Sutherland, G R; Reeders, S; Hyland, V J; Callen, D F; Fratini, A; Mulley, J C Journal: Journal of medical genetics Issue: Volume 24:Issue 8(1987) Page Start: 451 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. 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) ↗
9. Simultaneous trisomy 9q3 and monosomy 5p in two children with der(5), t(5;9)(p15.1;q34.13): report of an extended family. Issue 10 (October 1988) Authors: Wellesley, D; Young, I D; Cooke, P; Callen, D F; Hockey, A Journal: Journal of medical genetics Issue: Volume 25:Issue 10(1988) Page Start: 707 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) ↗