Showing results (251-260 of 299) with videos related to
Sort By:
Pageof 30
Oncogene|December 22, 2015
TBX2 represses PTEN in rhabdomyosarcoma and skeletal muscleB Zhu, M Zhang, E M Williams, et al.Clinical Genetics|March 1, 1997
Carrier screening for cystic fibrosis in primary care: evaluation of a project in South Wales. The South Wales Cystic Fibrosis Carrier Screening Research TeamY Payne, M Williams, J Cheadle, et al.Journal of Medical Genetics|September 1, 1991
Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17M C Koch, K Ricker, M Otto, et al.Human Genetics|November 1, 1991
Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17M C Koch, K Ricker, M Otto, et al.Journal of Medical Genetics|December 1, 1985
Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales familiesP S Harper, S Youngman, M A Anderson, et al.British Journal of Cancer|June 9, 1999
New classification of oesophageal and gastric carcinomas derived from changing patterns in epidemiologyK Dolan, R Sutton, S J Walker, et al.Clinical Science (London, England : 1979)|May 1, 1992
Effect of bicarbonate administration on skeletal muscle intracellular pH in the rat: implications for acute administration of bicarbonate in manC H Thompson, P D Syme, E M Williams, et al.Journal of Biomedical Engineering|September 1, 1993
Development of a concentric water-displacement model lungE M Williams, L B Gale, P A Oakley, et al.Nature|February 6, 1992
Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophyH G Harley, J D Brook, S A Rundle, et al.Human Genetics|May 1, 1991
Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19qH G Harley, K V Walsh, S Rundle, et al.Pageof 30