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M G Blitzer

Showing results (11-20 of 39) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1993
Transient neonatal galactosaemia identified by newborn screeningL J Raffel, T M Cowan, M G Blitzer
Maryland Medical Journal (Baltimore, Md. : 1985)|September 1, 1991
Study of the relationship between elevated maternal serum alpha-fetoprotein and adverse pregnancy outcomeA P Roop, J A Boughman, M G Blitzer
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 30, 1986
Discrimination of heterozygotes for phenylketonuria, persistent hyperphenylalaninemia and controls by phenylalanine loadingM G Blitzer, J E Bailey-Wilson, E Shapira
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 13, 1985
Discrimination of phenylketonurics from persistent hyperphenylalaninemia patients using a simple phenylalanine loading testM G Blitzer, J E Bailey-Wilson, E Shapira
American Journal of Medical Genetics|December 23, 1999
Summary of the Association of Professors of Human and Medical Genetics Fourth Annual WorkshopR J Desnick, B Korf, M G Blitzer, et al.
American Journal of Medical Genetics|March 1, 1985
A thermolabile variant of alpha-L-fucosidase--clinical and laboratory findingsM G Blitzer, M Sutton, J B Miller, et al.
American Journal of Medical Genetics|July 1, 1985
The "muscular variant" of Pompe disease: clinical, biochemical and histologic characteristicsJ K Temple, D W Dunn, M G Blitzer, et al.
Maryland Medical Journal (Baltimore, Md. : 1985)|November 1, 1989
Recent advances in geneticsM G Blitzer, S Schwartz, T M Cowan, et al.
Human Pathology|August 1, 1994
Biochemical diagnosis of fatty acid oxidation disorders by metabolite analysis of postmortem liverR G Boles, S K Martin, M G Blitzer, et al.
American Journal of Obstetrics and Gynecology|October 11, 1992
Multiple-marker screening in pregnancies with hydropic and nonhydropic Turner syndromeD N Saller, J A Canick, S Schwartz, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
Journal of Inherited Metabolic Disease|January 1, 1993
Transient neonatal galactosaemia identified by newborn screeningL J Raffel, T M Cowan, M G Blitzer
Maryland Medical Journal (Baltimore, Md. : 1985)|September 1, 1991
Study of the relationship between elevated maternal serum alpha-fetoprotein and adverse pregnancy outcomeA P Roop, J A Boughman, M G Blitzer
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 30, 1986
Discrimination of heterozygotes for phenylketonuria, persistent hyperphenylalaninemia and controls by phenylalanine loadingM G Blitzer, J E Bailey-Wilson, E Shapira
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 13, 1985
Discrimination of phenylketonurics from persistent hyperphenylalaninemia patients using a simple phenylalanine loading testM G Blitzer, J E Bailey-Wilson, E Shapira
American Journal of Medical Genetics|December 23, 1999
Summary of the Association of Professors of Human and Medical Genetics Fourth Annual WorkshopR J Desnick, B Korf, M G Blitzer, et al.
American Journal of Medical Genetics|March 1, 1985
A thermolabile variant of alpha-L-fucosidase--clinical and laboratory findingsM G Blitzer, M Sutton, J B Miller, et al.
American Journal of Medical Genetics|July 1, 1985
The "muscular variant" of Pompe disease: clinical, biochemical and histologic characteristicsJ K Temple, D W Dunn, M G Blitzer, et al.
Maryland Medical Journal (Baltimore, Md. : 1985)|November 1, 1989
Recent advances in geneticsM G Blitzer, S Schwartz, T M Cowan, et al.
Human Pathology|August 1, 1994
Biochemical diagnosis of fatty acid oxidation disorders by metabolite analysis of postmortem liverR G Boles, S K Martin, M G Blitzer, et al.
American Journal of Obstetrics and Gynecology|October 11, 1992
Multiple-marker screening in pregnancies with hydropic and nonhydropic Turner syndromeD N Saller, J A Canick, S Schwartz, et al.
Pageof 4