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Human Genetics|October 30, 1999
Long polymerase chain reaction in detection of germline deletions in the von Hippel-Lindau tumour suppressor geneC Cybulski, K Krzystolik, E R Maher, et al.Endocrinology|March 1, 1992
Evidence that the N-terminus of human growth hormone is involved in expression of its growth promoting, diabetogenic, and insulin-like activitiesR Towns, J L Kostyo, T Vogel, et al.Human Molecular Genetics|August 1, 1994
Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndromeW Reik, K W Brown, R E Slatter, et al.Free Radical Research Communications|January 1, 1987
The effect of systemic heparinisation and haemodialysis on plasma octadeca-9,11-dienoic acid (9,11-LA')D G Wickens, J F Griffin, E R Maher, et al.Human Molecular Genetics|December 1, 1995
Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domainW Reik, K W Brown, H Schneid, et al.American Journal of Human Genetics|October 3, 1998
An analysis of phenotypic variation in the familial cancer syndrome von Hippel-Lindau disease: evidence for modifier effectsA R Webster, F M Richards, F E MacRonald, et al.Genes, Chromosomes & Cancer|June 13, 1998
Inactivation of the von Hippel-Lindau (VHL) tumour suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: evidence for a VHL-independent pathway in clear cell renal tumourigenesisS C Clifford, A H Prowse, N A Affara, et al.Irish Journal of Medical Science|April 18, 2006
Demands for vascular access in a renal dialysis unit: implications for a regional vascular unitE Eguare, S Tierney, R Maher, et al.Ophthalmology|March 18, 1999
A clinical and molecular genetic analysis of solitary ocular angiomaA R Webster, E R Maher, A C Bird, et al.Molecular Genetics and Metabolism|December 17, 2009
A novel PCFT gene mutation (p.Cys66LeufsX99) causing hereditary folate malabsorptionEsther Meyer, Manju A Kurian, Shanaz Pasha, et al.Pageof 63