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N Fischel-Ghodsian

Showing results (1-10 of 85) with videos related to

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Molecular Genetics and Metabolism|September 26, 2000
Homoplasmic mitochondrial DNA diseases as the paradigm to understand the tissue specificity and variable clinical severity of mitochondrial disordersN Fischel-Ghodsian
Annals of Internal Medicine|May 1, 2001
Mitochondrial DNA mutations and diabetes: another step toward individualized medicineN Fischel-Ghodsian
American Journal of Human Genetics|March 7, 1998
Mitochondrial mutations and hearing loss: paradigm for mitochondrial geneticsN Fischel-Ghodsian
Molecular Genetics and Metabolism|October 27, 1998
Mitochondrial RNA processing and translation: link between mitochondrial mutations and hearing loss?N Fischel-Ghodsian
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|May 8, 1998
Mitochondrial genetics and hearing loss: the missing link between genotype and phenotypeN Fischel-Ghodsian
Annals of the New York Academy of Sciences|June 8, 2000
Genetic factors in aminoglycoside toxicityN Fischel-Ghodsian
Human Mutation|April 29, 1999
Mitochondrial deafness mutations reviewedN Fischel-Ghodsian
Clinics in Perinatology|December 1, 1990
Prenatal diagnosis of hemoglobinopathiesN Fischel-Ghodsian
Human Mutation|January 1, 1992
Trapped-oligonucleotide nucleotide incorporation (TONI) assay, a simple method for screening point mutationsT R Prezant, N Fischel-Ghodsian
Human Molecular Genetics|August 1, 2000
A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicityM X Guan, N Fischel-Ghodsian, G Attardi
Pageof 9

Showing results (1-10 of 85) with videos related to

Sort By:
Pageof 9
Molecular Genetics and Metabolism|September 26, 2000
Homoplasmic mitochondrial DNA diseases as the paradigm to understand the tissue specificity and variable clinical severity of mitochondrial disordersN Fischel-Ghodsian
Annals of Internal Medicine|May 1, 2001
Mitochondrial DNA mutations and diabetes: another step toward individualized medicineN Fischel-Ghodsian
American Journal of Human Genetics|March 7, 1998
Mitochondrial mutations and hearing loss: paradigm for mitochondrial geneticsN Fischel-Ghodsian
Molecular Genetics and Metabolism|October 27, 1998
Mitochondrial RNA processing and translation: link between mitochondrial mutations and hearing loss?N Fischel-Ghodsian
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)|May 8, 1998
Mitochondrial genetics and hearing loss: the missing link between genotype and phenotypeN Fischel-Ghodsian
Annals of the New York Academy of Sciences|June 8, 2000
Genetic factors in aminoglycoside toxicityN Fischel-Ghodsian
Human Mutation|April 29, 1999
Mitochondrial deafness mutations reviewedN Fischel-Ghodsian
Clinics in Perinatology|December 1, 1990
Prenatal diagnosis of hemoglobinopathiesN Fischel-Ghodsian
Human Mutation|January 1, 1992
Trapped-oligonucleotide nucleotide incorporation (TONI) assay, a simple method for screening point mutationsT R Prezant, N Fischel-Ghodsian
Human Molecular Genetics|August 1, 2000
A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicityM X Guan, N Fischel-Ghodsian, G Attardi
Pageof 9