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N E Simpson

Showing results (1-10 of 91) with videos related to

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Canadian Family Physician Medecin De Famille Canadien|May 15, 2010
Family tree research programN E Simpson
Journal of Medical Genetics|December 1, 1988
The map of chromosome 20N E Simpson
Henry Ford Hospital Medical Journal|January 1, 1984
Genetic studies of multiple endocrine neoplasia type 2 syndromes: a workshop commentaryN E Simpson
Canadian Medical Association Journal|March 24, 2010
Prenatal diagnosis of genetic diseaseN E Simpson
American Journal of Medical Genetics|January 1, 1986
Dermatoglyphic indices of males with the fragile X syndrome and of the female heterozygotesN E Simpson
Internationale Zeitschrift Fur Klinische Pharmakologie, Therapie, Und Toxikologie. International Journal of Clinical Pharmacology, Therapy, and Toxicology|August 1, 1971
A geneticist's look at pharmacogeneticsN E Simpson
American Journal of Human Genetics|May 1, 1972
Polyacrylamide electrophoresis used for the detection of C5+ cholinesterase in Canadian caucasians, Indians, and EskimosN E Simpson
Isozymes|January 1, 1983
Prenatal diagnosis of neural tube defects using the cholinesterasesN E Simpson
Canadian Journal of Genetics and Cytology. Journal Canadien De Genetique Et De Cytologie|January 1, 1980
The genetics of diabetes mellitus in manN E Simpson
Journal of Medical Genetics|December 1, 1975
Letter: Mutation as the source of the abnormal gene for plasma cholinesteraseN E Simpson
Pageof 10

Showing results (1-10 of 91) with videos related to

Sort By:
Pageof 10
Canadian Family Physician Medecin De Famille Canadien|May 15, 2010
Family tree research programN E Simpson
Journal of Medical Genetics|December 1, 1988
The map of chromosome 20N E Simpson
Henry Ford Hospital Medical Journal|January 1, 1984
Genetic studies of multiple endocrine neoplasia type 2 syndromes: a workshop commentaryN E Simpson
Canadian Medical Association Journal|March 24, 2010
Prenatal diagnosis of genetic diseaseN E Simpson
American Journal of Medical Genetics|January 1, 1986
Dermatoglyphic indices of males with the fragile X syndrome and of the female heterozygotesN E Simpson
Internationale Zeitschrift Fur Klinische Pharmakologie, Therapie, Und Toxikologie. International Journal of Clinical Pharmacology, Therapy, and Toxicology|August 1, 1971
A geneticist's look at pharmacogeneticsN E Simpson
American Journal of Human Genetics|May 1, 1972
Polyacrylamide electrophoresis used for the detection of C5+ cholinesterase in Canadian caucasians, Indians, and EskimosN E Simpson
Isozymes|January 1, 1983
Prenatal diagnosis of neural tube defects using the cholinesterasesN E Simpson
Canadian Journal of Genetics and Cytology. Journal Canadien De Genetique Et De Cytologie|January 1, 1980
The genetics of diabetes mellitus in manN E Simpson
Journal of Medical Genetics|December 1, 1975
Letter: Mutation as the source of the abnormal gene for plasma cholinesteraseN E Simpson
Pageof 10