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The Journal of Endocrinology|April 10, 2004
Beta cell differentiation during early human pancreas developmentK Piper, S Brickwood, L W Turnpenny, et al.Annals of Clinical Biochemistry|April 21, 1998
Simplified detection of a mutation causing familial hypercholesterolaemia throughout Britain: evidence for an origin in a common distant ancestorP R Wenham, L Haddad, M Panarelli, et al.Disease Markers|April 29, 1998
Analysis of the association of a heat shock protein70-1 gene promoter polymorphism with myocardial infarction and coronary risk traitsM K Bolla, G J Miller, D M Yellon, et al.Journal of Medical Genetics|July 25, 1998
Identification of a common low density lipoprotein receptor mutation (C163Y) in the west of ScotlandW K Lee, L Haddad, M J Macleod, et al.Human Molecular Genetics|October 1, 1993
Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndromeS Halford, D I Wilson, S C Daw, et al.Lancet (London, England)|May 9, 1992
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locusP J Scambler, D Kelly, E Lindsay, et al.Mechanisms of Development|September 24, 1999
Expression of steroidogenic factor 1 and Wilms' tumour 1 during early human gonadal development and sex determinationN A Hanley, S G Ball, M Clement-Jones, et al.American Journal of Human Genetics|November 1, 1992
A prospective cytogenetic study of 36 cases of DiGeorge syndromeD I Wilson, I E Cross, J A Goodship, et al.Journal of Neurology, Neurosurgery, and Psychiatry|April 19, 2005
Rate of progression of cognitive decline in Alzheimer's disease: effect of butyrylcholinesterase K gene variationC Holmes, C Ballard, D Lehmann, et al.British Heart Journal|October 1, 1991
DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal originD I Wilson, I E Cross, J A Goodship, et al.Pageof 12