1. A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13. Issue 6 (1st June 2003) Authors: Morgan, N V; Bacchelli, C; Gissen, P; Morton, J; Ferrero, G B; Silengo, M; Labrune, P; Casteels, I; Hall, C; Cox, P; Kelly, D A; Trembath, R C; Scambler, P J; Maher, E R; Goodman, F R; Johnson, C A Journal: Journal of medical genetics Issue: Volume 40:Issue 6(2003) Page Start: 431 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Albright's hereditary osteodystrophy. Issue 10 (October 1994) Authors: Wilson, L C; Trembath, R C Journal: Journal of medical genetics Issue: Volume 31:Issue 10(1994) Page Start: 779 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. BMPRII deficiency impairs apoptosis via the BMPRII-ALK1-BclX-mediated pathway in pulmonary arterial hypertension. (27th February 2019) Authors: Chowdhury, H M; Sharmin, N; Yuzbasioglu Baran, Merve; Long, L; Morrell, N W; Trembath, R C; Nasim, Md Talat Journal: Human molecular genetics Issue: Volume 28:Number 13(2019) Page Start: 2161 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Compound heterozygous ZMPSTE24 mutations reduce prelamin A processing and result in a severe progeroid phenotype. Issue 6 (3rd June 2005) Authors: Shackleton, S; Smallwood, D T; Clayton, P; Wilson, L C; Agarwal, A K; Garg, A; Trembath, R C Journal: Journal of medical genetics Issue: Volume 42:Issue 6(2005) Page Start: e36 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Deoxyribonucleic acid polymorphism of the apoprotein AI-CIII-AIV gene cluster and coronary heart disease in non-insulin-dependent diabetes. Issue 6587 (20th June 1987) Authors: Trembath, R C; Thomas, D J; Hendra, T J; Yudkin, J S; Galton, D J Journal: BMJ Issue: Volume 294:Issue 6587(1987) Page Start: 1577 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Effect of octreotide on gall stone prevalence and gall bladder motility in acromegaly. Issue 2 (February 1993) Authors: Catnach, S M; Anderson, J V; Fairclough, P D; Trembath, R C; Wilson, P A; Parker, E; Besser, G M; Wass, J A Journal: Gut Issue: Volume 34:Issue 2(1993) Page Start: 270 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Erythromycin induces supranormal gall bladder contraction in diabetic autonomic neuropathy. Issue 8 (August 1993) Authors: Catnach, S M; Ballinger, A B; Stevens, M; Fairclough, P D; Trembath, R C; Drury, P L; Watkins, P J Journal: Gut Issue: Volume 34:Issue 8(1993) Page Start: 1123 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype. Issue 8 (1st August 1999) Authors: Bijlsma, E K; Aalfs, C M; Sluijter, S; Luttikhuis, M E M Oude; Trembath, R C; Hoovers, J M N; Hennekam, R C M Journal: Journal of medical genetics Issue: Volume 36:Issue 8(1999) Page Start: 604 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Genetic analysis of PSORS2 markers in a UK dataset supports the association between RAPTOR SNPs and familial psoriasis. Issue 6 (1st June 2004) Authors: Capon, F; Helms, C; Veal, C D; Tillman, D; Burden, A D; Barker, J N; Bowcock, A M; Trembath, R C Journal: Journal of medical genetics Issue: Volume 41:Issue 6(2004) Page Start: 459 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Genomic duplication in Dyggve Melchior Clausen syndrome, a novel mutation mechanism in an autosomal recessive disorder. Issue 12 (2nd December 2005) Authors: Kinning, E; Tufarelli, C; Winship, W S; Aldred, M A; Trembath, R C Journal: Journal of medical genetics Issue: Volume 42:Issue 12(2005) Page Start: e70 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗