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J E SPENCE

Showing results (31-40 of 51) with videos related to

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American Journal of Medical Genetics|August 1, 1992
Parental origin determination in thirty de novo Robertsonian translocationsL G Shaffer, C K Jackson-Cook, B A Stasiowski, et al.
Canadian Journal of Physiology and Pharmacology|October 1, 1987
Endometrial prostaglandins and menorrhagia: influence of a prostaglandin synthetase inhibitor in vivoB K Tsang, M T Domingo, J E Spence, et al.
Fertility and Sterility|January 1, 1997
A randomized clinical trial of oxidized regenerated cellulose adhesion barrier (Interceed, TC7) alone or in combination with heparinR L Reid, P M Hahn, J E Spence, et al.
The New England Journal of Medicine|January 7, 1988
Experience with new DNA markers for the diagnosis of cystic fibrosisA L Beaudet, J E Spence, M Montes, et al.
Neuromuscular Disorders : NMD|March 11, 2000
Two distal mutations in the gene encoding emerin have profoundly different effects on emerin protein expressionJ A Ellis, C A Brown, L D Tilley, et al.
Cytogenetics and Cell Genetics|January 1, 1987
Exclusion of close linkage between the loci for cystic fibrosis and neuropeptide Y on human chromosome 7M H Meisler, J E Spence, J E Dixon, et al.
Clinical Chemistry|May 1, 1988
Prenatal diagnosis of cystic fibrosis: microvillar enzymes and DNA analysis comparedG J Buffone, J E Spence, S D Fernbach, et al.
Annals of Neurology|September 1, 1986
Atypical presentation and neuropathological studies in 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyH Y Zoghbi, J E Spence, A L Beaudet, et al.
The Journal of Pediatrics|April 1, 1989
Prenatal diagnosis and heterozygote detection by DNA analysis in ornithine transcarbamylase deficiencyJ E Spence, A Maddalena, W E O'Brien, et al.
The Journal of Biological Chemistry|March 4, 1994
Human serum biotinidase. cDNA cloning, sequence, and characterizationH Cole, T R Reynolds, J M Lockyer, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics|August 1, 1992
Parental origin determination in thirty de novo Robertsonian translocationsL G Shaffer, C K Jackson-Cook, B A Stasiowski, et al.
Canadian Journal of Physiology and Pharmacology|October 1, 1987
Endometrial prostaglandins and menorrhagia: influence of a prostaglandin synthetase inhibitor in vivoB K Tsang, M T Domingo, J E Spence, et al.
Fertility and Sterility|January 1, 1997
A randomized clinical trial of oxidized regenerated cellulose adhesion barrier (Interceed, TC7) alone or in combination with heparinR L Reid, P M Hahn, J E Spence, et al.
The New England Journal of Medicine|January 7, 1988
Experience with new DNA markers for the diagnosis of cystic fibrosisA L Beaudet, J E Spence, M Montes, et al.
Neuromuscular Disorders : NMD|March 11, 2000
Two distal mutations in the gene encoding emerin have profoundly different effects on emerin protein expressionJ A Ellis, C A Brown, L D Tilley, et al.
Cytogenetics and Cell Genetics|January 1, 1987
Exclusion of close linkage between the loci for cystic fibrosis and neuropeptide Y on human chromosome 7M H Meisler, J E Spence, J E Dixon, et al.
Clinical Chemistry|May 1, 1988
Prenatal diagnosis of cystic fibrosis: microvillar enzymes and DNA analysis comparedG J Buffone, J E Spence, S D Fernbach, et al.
Annals of Neurology|September 1, 1986
Atypical presentation and neuropathological studies in 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyH Y Zoghbi, J E Spence, A L Beaudet, et al.
The Journal of Pediatrics|April 1, 1989
Prenatal diagnosis and heterozygote detection by DNA analysis in ornithine transcarbamylase deficiencyJ E Spence, A Maddalena, W E O'Brien, et al.
The Journal of Biological Chemistry|March 4, 1994
Human serum biotinidase. cDNA cloning, sequence, and characterizationH Cole, T R Reynolds, J M Lockyer, et al.
Pageof 6