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The American Journal of Medicine|July 1, 1979
Familial recurrent rhabdomyolysis due to carnitine palmityl transferase deficiencyB M Patten, J M Wood, Y Harati, et al.The American Journal of Cardiology|January 1, 1988
Echocardiographic abnormalities in the mucopolysaccharide storage diseasesD M Gross, J C Williams, C Caprioli, et al.Science (New York, N.Y.)|September 11, 1992
Volcanic Activity on lo at the Time of the Ulysses EncounterJ R Spencer, R R Howell, B E Clark, et al.Birth Defects Original Article Series|January 1, 1976
A syndrome manifested by brittle hair with morphologic and biochemical abnormalities, developmental delay and normal statureA I Arbisser, C I Scott, R R Howell, et al.Hybridoma|January 1, 1985
Detection of human acid alpha-glucosidase in fibroblasts using monoclonal antibodies in a biotin-avidin amplified ELISAR D Henkel, G R Dreesman, R C Kennedy, et al.JAMA|September 27, 1976
Hepatic adenomata with type 1 glycogen storage diseaseR R Howell, R E Stevenson, Y Ben-Menachem, et al.Science (New York, N.Y.)|October 8, 1971
Xeroderma pigmentosum: a rapid sensitive method for prenatal diagnosisJ D Regan, R B Setlow, M M Kaback, et al.Pediatrics|January 1, 1976
The iduronidase-deficient mucopolysaccharidoses: clinical and roentgenorgraphic featuresR E Stevenson, R R Howell, V A McKusick, et al.American Journal of Medical Genetics|January 1, 1977
Morquio-like syndrome with beta galactosidase deficiency and normal hexosamine sulfatase activity: mucopolysacchariodosis IVBA I Arbisser, K A Donnelly, C I Scott, et al.American Journal of Human Genetics|November 1, 1981
The Sabinas syndromeR R Howell, A I Arbisser, D S Parsons, et al.Pageof 4