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R R Frants

Showing results (41-50 of 282) with videos related to

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Bulletin Du Cancer|September 30, 1998
Genetics of familial atypical multiple mole-melanoma (FAMMM) syndrome in The Netherlands: how far have we come?N A Gruis, P A Van der Velden, W Bergman, et al.
Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie. Albrecht Von Graefe'S Archive for Clinical and Experimental Ophthalmology|January 1, 1981
Alpha 1-antitrypsin and acute anterior uveitisK M Saari, J Solja, M Sirpelä, et al.
Biochemical Society Transactions|May 1, 1996
A search for genes in the facioscapulohumeral muscular dystrophy regionP K Grewal, J C Van Deutekom, R R Frants, et al.
Muscle & Nerve. Supplement|April 12, 2013
Early onset facioscapulohumeral muscular dystrophyO F Brouwer, G W Padberg, E Bakker, et al.
Human Mutation|January 1, 1994
Genetic heterogeneity of apolipoprotein E and its influence on plasma lipid and lipoprotein levelsP de Knijff, A M van den Maagdenberg, R R Frants, et al.
Biochemical Genetics|February 1, 1986
Variant-specific differences in human unsaturated transcobalamin IIH J Porck, R R Frants, J Lindemans, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 12, 1998
[Channelopathies: a genetic explanation of migraine and other paroxysmal neurologic disorders]G M Terwindt, R A Ophoff, J Haan, et al.
Cephalalgia : an International Journal of Headache|May 1, 1996
Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RGG M Terwindt, R A Ophoff, J Haan, et al.
Annales Academiae Scientiarum Fennicae. Ser. A.5, Medica|January 1, 1986
Genetic polymorphisms in serum and erythrocytes of the BashkirsR R Frants, M Kirjarinta, P M Khan, et al.
Clinical Genetics|November 1, 1987
Familial dysbetalipoproteinemic subjects with the E3/E2 phenotype exhibit an E2 isoform with only one cysteine residueM Smit, P de Knijff, R R Frants, et al.
Pageof 29

Showing results (41-50 of 282) with videos related to

Sort By:
Pageof 29
Bulletin Du Cancer|September 30, 1998
Genetics of familial atypical multiple mole-melanoma (FAMMM) syndrome in The Netherlands: how far have we come?N A Gruis, P A Van der Velden, W Bergman, et al.
Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie. Albrecht Von Graefe'S Archive for Clinical and Experimental Ophthalmology|January 1, 1981
Alpha 1-antitrypsin and acute anterior uveitisK M Saari, J Solja, M Sirpelä, et al.
Biochemical Society Transactions|May 1, 1996
A search for genes in the facioscapulohumeral muscular dystrophy regionP K Grewal, J C Van Deutekom, R R Frants, et al.
Muscle & Nerve. Supplement|April 12, 2013
Early onset facioscapulohumeral muscular dystrophyO F Brouwer, G W Padberg, E Bakker, et al.
Human Mutation|January 1, 1994
Genetic heterogeneity of apolipoprotein E and its influence on plasma lipid and lipoprotein levelsP de Knijff, A M van den Maagdenberg, R R Frants, et al.
Biochemical Genetics|February 1, 1986
Variant-specific differences in human unsaturated transcobalamin IIH J Porck, R R Frants, J Lindemans, et al.
Nederlands Tijdschrift Voor Geneeskunde|June 12, 1998
[Channelopathies: a genetic explanation of migraine and other paroxysmal neurologic disorders]G M Terwindt, R A Ophoff, J Haan, et al.
Cephalalgia : an International Journal of Headache|May 1, 1996
Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RGG M Terwindt, R A Ophoff, J Haan, et al.
Annales Academiae Scientiarum Fennicae. Ser. A.5, Medica|January 1, 1986
Genetic polymorphisms in serum and erythrocytes of the BashkirsR R Frants, M Kirjarinta, P M Khan, et al.
Clinical Genetics|November 1, 1987
Familial dysbetalipoproteinemic subjects with the E3/E2 phenotype exhibit an E2 isoform with only one cysteine residueM Smit, P de Knijff, R R Frants, et al.
Pageof 29