1. A homozygote for pericentric inversion of chromosome 4. Issue 6 (December 1982) Authors: Carpenter, N J; Say, B; Barber, N D Journal: Journal of medical genetics Issue: Volume 19:Issue 6(1982) Page Start: 469 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Agenesis of the lung associated with a chromosome abnormality (46, XX, 2p+). Issue 6 (December 1980) Authors: Say, B; Carpenter, N J; Giacoia, G; Jegathesan, S Journal: Journal of medical genetics Issue: Volume 17:Issue 6(1980) Page Start: 477 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. An infant with multiple congenital abnormalities and biochemical findings suggesting a variant of galactosialidosis. Issue 6 (June 1992) Authors: Say, B; Hommes, F A; Malik, S A; Carpenter, N J Journal: Journal of medical genetics Issue: Volume 29:Issue 6(1992) Page Start: 423 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. An infant with ring 17 chromosome and unusual dermatoglyphs: a new syndrome?. Issue 3 (June 1981) Authors: Carpenter, N J; Leichtman, L G; Stamper, S; Say, B Journal: Journal of medical genetics Issue: Volume 18:Issue 3(1981) Page Start: 234 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. An unusual chromosomal aberration in a case of Chediak-Higashi syndrome. Issue 4 (December 1970) Authors: Say, B; Tunçbilek, E; Yamak, B; Balci, S Journal: Journal of medical genetics Issue: Volume 7:Issue 4(1970) Page Start: 417 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Aspects of pre-eclamptic toxaemia of pregnancy, consanguinity, twinning in Ankara. Issue 1 (February 1976) Authors: Stevenson, A C; Say, B; Ustaoglu, S; Durmus, Z Journal: Journal of medical genetics Issue: Volume 13:Issue 1(1976) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Detection of a familial cryptic translocation by fluorescent in situ hybridisation. Issue 1 (January 1996) Authors: Smith, D P; Floyd, M; Say, B Journal: Journal of medical genetics Issue: Volume 33:Issue 1(1996) Page Start: 84 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Gonadal dysgenesis in a patient with an X;3 translocation: case report and review. Issue 3 (June 1980) Authors: Carpenter, N J; Say, B; Browning, D Journal: Journal of medical genetics Issue: Volume 17:Issue 3(1980) Page Start: 216 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Mental retardation with blepharophimosis. Issue 8 (August 1987) Authors: Say, B; Barber, N Journal: Journal of medical genetics Issue: Volume 24:Issue 8(1987) Page Start: 511 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Microcephaly, short stature, and developmental delay associated with a chemotactic defect and transient hypogammaglobulinaemia in two brothers. Issue 4 (August 1986) Authors: Say, B; Barber, N; Miller, G C; Grogg, S E Journal: Journal of medical genetics Issue: Volume 23:Issue 4(1986) Page Start: 355 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗