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Annals of Human Genetics|May 1, 1989
Isozyme and DNA analysis of human S-adenosyl-L-homocysteine hydrolase (AHCY)F X Arredondo-Vega, J A Charlton, Y H Edwards, et al.Clinical Chemistry|October 24, 2001
Identification of alpha(1)-antitrypsin variants in plasma with the use of proteomic technologyK Mills, P B Mills, P T Clayton, et al.Prenatal Diagnosis|February 1, 1987
Prenatal diagnosis of alpha-1-antitrypsin deficiency by fetal blood samplingG Corney, D B Whitehouse, D A Hopkinson, et al.Hepatology (Baltimore, Md.)|August 1, 1990
HLA phenotypes and gene polymorphisms in juvenile liver disease associated with alpha 1-antitrypsin deficiencyD G Doherty, P T Donaldson, D B Whitehouse, et al.British Journal of Obstetrics and Gynaecology|March 1, 1994
Lack of association between maternal phosphoglucomutase-1 phenotype and fetal macrosomia in diabetic pregnancyF D Johnstone, J D West, J Steel, et al.Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
Phosphoglucomutase 1: complete human and rabbit mRNA sequences and direct mapping of this highly polymorphic marker on human chromosome 1D B Whitehouse, W Putt, J U Lovegrove, et al.Proceedings of the National Academy of Sciences of the United States of America|November 15, 1993
The classical human phosphoglucomutase (PGM1) isozyme polymorphism is generated by intragenic recombinationR E March, W Putt, M Hollyoake, et al.Journal of Medical Genetics|December 1, 1989
Genetic studies on a new deficiency gene (PI*Ztun) at the PI locusD B Whitehouse, C M Abbott, J U Lovegrove, et al.American Journal of Human Genetics|March 1, 1986
A population genetic survey of the haptoglobin polymorphism in Melanesians by DNA analysisA V Hill, D K Bowden, J Flint, et al.Disease Markers|December 1, 1993
Fetal growth, gestation length and phosphoglucomutase-1 phenotypeF D Johnstone, J D West, R J Prescott, et al.Pageof 5