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Human Molecular Genetics|February 1, 1995
A radiographic, morphologic, biochemical and molecular analysis of a case of achondrogenesis type II resulting from substitution for a glycine residue (Gly691-->Arg) in the type II collagen trimerG R Mortier, D J Wilkin, W R Wilcox, et al.The New England Journal of Medicine|January 11, 1979
Duodenal-ulcer disease associated with elevated serum pepsinogen I: an inherited autosomal dominant disorderJ I Rotter, J Q Sones, I M Samloff, et al.American Journal of Medical Genetics|January 1, 1980
Congenital macular colobomas and short-limb skeletal dysplasiaR D Smith, R M Fineman, D O Sillence, et al.Developmental Psychobiology|January 11, 1976
Audiogenic priming in DBA/2J and C57BL/6J mice: interactions among age, prime-to-test interval and index of seizureR A Schreiber, J M GrahamAmerican Journal of Surgery|August 1, 1987
Diagnostic and surgical considerations in the treatment of thoracoabdominal and suprarenal aortic aneurysmsJ M Graham, D M StinnettThe Biochemical Journal|June 1, 1988
Subcellular localization of the sulphation reaction of heparan sulphate synthesis and transport of the proteoglycan to the cell surface in rat liverJ M Graham, D J WinterbourneThe Journal of Physiology|May 1, 1975
Responses of inner and outer muscle of the sheep carotid artery to injuryJ M Graham, W R KeatingeMovement Disorders : Official Journal of the Movement Disorder Society|January 26, 1999
A data-driven approach to the study of heterogeneity in idiopathic Parkinson's disease: identification of three distinct subtypesJ M Graham, H J SagarPostgraduate Medical Journal|January 1, 1978
Chronic active hepatitis, haemolytic anaemia and Listeria monocytogenes bacteraemiaR G Chadwick, J M GrahamPageof 42