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P D Murphy

Showing results (11-20 of 31) with videos related to

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American Journal of Medical Genetics|April 1, 1992
Prenatal diagnosis of fragile X syndrome: results from parallel molecular and cytogenetic studiesP D Murphy, P L Wilmot, L R Shapiro
Cytogenetics and Cell Genetics|January 1, 1985
Quantitation of the transgenome size in chromosome-mediated gene transfer linesP D Murphy, C L Miller, F H Ruddle
Muscle & Nerve|January 1, 1995
A retrospective study of 47 patients with highly elevated anti-GM1 antibodiesM A Boss, U Ananth, D Paquet, et al.
The Journal of Experimental Medicine|April 1, 1978
T cells specific for hapten-modified self are precommitted for self major histocompatibility complex antigens before encounter with the haptenC A Janeway, P D Murphy, J Kemp, et al.
Biochemical Medicine and Metabolic Biology|October 1, 1993
Molecular confirmation of alpha 1-antitrypsin genotypes in newborn dried blood specimensW C Spence, J E Morris, K Pass, et al.
Irish Medical Journal|May 1, 1986
Adenocarcinoma of the duodenum and iron deficiency anaemiaD P Watson, P D Murphy, T M Feeley, et al.
Genetic Testing|January 1, 1997
The Oncormed approach to genetic testingC L Carter, J A Scott, P M Glauber, et al.
Nucleic Acids Research|September 11, 1987
A second useful polymorphism for the cytosolic thymidine kinase gene (TK1) with the enzyme BstEII which will allow haplotying at this locus on chromosome 17 (q21-q22)P D Murphy, P F Lin, F H Ruddle, et al.
Science (New York, N.Y.)|February 12, 1998
Predictive genetic testing: from basic research to clinical practiceN A Holtzman, P D Murphy, M S Watson, et al.
American Journal of Medical Genetics|May 1, 1988
Experience with multiple approaches to the prenatal diagnosis of the fragile X syndrome: amniotic fluid, chorionic villi, fetal blood and molecular methodsL R Shapiro, P L Wilmot, P D Murphy, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|April 1, 1992
Prenatal diagnosis of fragile X syndrome: results from parallel molecular and cytogenetic studiesP D Murphy, P L Wilmot, L R Shapiro
Cytogenetics and Cell Genetics|January 1, 1985
Quantitation of the transgenome size in chromosome-mediated gene transfer linesP D Murphy, C L Miller, F H Ruddle
Muscle & Nerve|January 1, 1995
A retrospective study of 47 patients with highly elevated anti-GM1 antibodiesM A Boss, U Ananth, D Paquet, et al.
The Journal of Experimental Medicine|April 1, 1978
T cells specific for hapten-modified self are precommitted for self major histocompatibility complex antigens before encounter with the haptenC A Janeway, P D Murphy, J Kemp, et al.
Biochemical Medicine and Metabolic Biology|October 1, 1993
Molecular confirmation of alpha 1-antitrypsin genotypes in newborn dried blood specimensW C Spence, J E Morris, K Pass, et al.
Irish Medical Journal|May 1, 1986
Adenocarcinoma of the duodenum and iron deficiency anaemiaD P Watson, P D Murphy, T M Feeley, et al.
Genetic Testing|January 1, 1997
The Oncormed approach to genetic testingC L Carter, J A Scott, P M Glauber, et al.
Nucleic Acids Research|September 11, 1987
A second useful polymorphism for the cytosolic thymidine kinase gene (TK1) with the enzyme BstEII which will allow haplotying at this locus on chromosome 17 (q21-q22)P D Murphy, P F Lin, F H Ruddle, et al.
Science (New York, N.Y.)|February 12, 1998
Predictive genetic testing: from basic research to clinical practiceN A Holtzman, P D Murphy, M S Watson, et al.
American Journal of Medical Genetics|May 1, 1988
Experience with multiple approaches to the prenatal diagnosis of the fragile X syndrome: amniotic fluid, chorionic villi, fetal blood and molecular methodsL R Shapiro, P L Wilmot, P D Murphy, et al.
Pageof 4