Showing results (1-10 of 12) with videos related to
Sort By:
Pageof 2
The British Journal of Dermatology|January 22, 2011
Preliminary evidence for involvement of the tumour suppressor gene CHD5 in a family with cutaneous melanomaJ Lang, E S Tobias, R MackieSeizure|March 1, 1994
An outcome audit at the epilepsy clinic: results from 1000 consecutive referralsE S Tobias, A F Brodie, M J BrodieThe Biochemical Journal|September 18, 1997
Co-transfection with protein kinase D confers phorbol-ester-mediated inhibition on glucagon-stimulated cAMP accumulation in COS cells transfected to overexpress glucagon receptorsE S Tobias, E Rozengurt, J M Connell, et al.Archives of Disease in Childhood|November 26, 1999
Towards earlier diagnosis of 22q11 deletionsE S Tobias, N Morrison, M L Whiteford, et al.Clinical Dysmorphology|January 11, 2001
A case of Acro-renal-mandibular syndrome in an 18 week male fetusE S Tobias, Patrick WJA, J R MacKenzie, et al.Oncogene|June 23, 2001
The TES gene at 7q31.1 is methylated in tumours and encodes a novel growth-suppressing LIM domain proteinE S Tobias, A F Hurlstone, E MacKenzie, et al.Nature Genetics|December 1, 2001
Absence of ST7 mutations in tumor-derived cell lines and tumorsK A Hughes, A F Hurlstone, E S Tobias, et al.European Journal of Endocrinology|July 23, 2017
Androgen-responsive non-coding small RNAs extend the potential of HCG stimulation to act as a bioassay of androgen sufficiencyM E Rodie, M A V Mudaliar, P Herzyk, et al.Familial Cancer|September 1, 2006
Gastric carcinoid: germline and somatic mutation of the neurofibromatosis type 1 geneW Stewart, J P Traynor, A Cooke, et al.Journal of Medical Genetics|July 17, 2008
Cerebro-oculo-facio-skeletal syndrome: three additional cases with CSB mutations, new diagnostic criteria and an approach to investigationV Laugel, C Dalloz, E S Tobias, et al.Pageof 2