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R R Frants

Showing results (21-30 of 282) with videos related to

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British Journal of Cancer|February 1, 1981
M2 alpha-1-antitrypsin phenotype and primary liver cancerP Sizaret, M Clerc, J Estève, et al.
Lancet (London, England)|October 17, 1992
Transmission of de-novo mutation associated with facioscapulohumeral muscular dystrophyC Wijmenga, O F Brouwer, G W Padberg, et al.
Archives of Neurology|April 1, 1994
Facioscapulohumeral muscular dystrophy in early childhoodO F Brouwer, G W Padberg, C Wijmenga, et al.
Molecular and Cell Biology of Human Diseases Series|January 1, 1993
Genetic mapping of facioscapulohumeral muscular dystrophyC Wijmenga, M H Hofker, G W Padberg, et al.
The Journal of Investigative Dermatology|November 1, 1994
Genetics of seven Dutch familial atypical multiple mole-melanoma syndrome families: a review of linkage results including chromosomes 1 and 9W Bergman, N A Gruis, L A Sandkuijl, et al.
Advances in Experimental Medicine and Biology|January 1, 1988
The effect of apolipoprotein E allele substitutions on plasma lipid and apolipoprotein levelsL M Havekes, P de Knijff, M Smit, et al.
Clinical Neurology and Neurosurgery|March 1, 1993
Facioscapulohumeral muscular dystrophy: the impact of genetic researchO F Brouwer, C Wijmenga, R R Frants, et al.
Biochimica Et Biophysica Acta|May 1, 1990
Characterisation of the LDL receptor in Epstein-Barr virus transformed lymphocytesP Lombardi, E de Wit, R R Frants, et al.
Lancet (London, England)|January 28, 1978
Erythrocyte superoxide-dismutase deficiency in Fanconi's anaemiaH Joenje, A W Eriksson, R R Frants, et al.
Clinical Genetics|July 1, 1990
Pseudoinflammatory fundus dystrophy: a follow-up studyA W Eriksson, E A Suvanto, R R Frants, et al.
Pageof 29

Showing results (21-30 of 282) with videos related to

Sort By:
Pageof 29
British Journal of Cancer|February 1, 1981
M2 alpha-1-antitrypsin phenotype and primary liver cancerP Sizaret, M Clerc, J Estève, et al.
Lancet (London, England)|October 17, 1992
Transmission of de-novo mutation associated with facioscapulohumeral muscular dystrophyC Wijmenga, O F Brouwer, G W Padberg, et al.
Archives of Neurology|April 1, 1994
Facioscapulohumeral muscular dystrophy in early childhoodO F Brouwer, G W Padberg, C Wijmenga, et al.
Molecular and Cell Biology of Human Diseases Series|January 1, 1993
Genetic mapping of facioscapulohumeral muscular dystrophyC Wijmenga, M H Hofker, G W Padberg, et al.
The Journal of Investigative Dermatology|November 1, 1994
Genetics of seven Dutch familial atypical multiple mole-melanoma syndrome families: a review of linkage results including chromosomes 1 and 9W Bergman, N A Gruis, L A Sandkuijl, et al.
Advances in Experimental Medicine and Biology|January 1, 1988
The effect of apolipoprotein E allele substitutions on plasma lipid and apolipoprotein levelsL M Havekes, P de Knijff, M Smit, et al.
Clinical Neurology and Neurosurgery|March 1, 1993
Facioscapulohumeral muscular dystrophy: the impact of genetic researchO F Brouwer, C Wijmenga, R R Frants, et al.
Biochimica Et Biophysica Acta|May 1, 1990
Characterisation of the LDL receptor in Epstein-Barr virus transformed lymphocytesP Lombardi, E de Wit, R R Frants, et al.
Lancet (London, England)|January 28, 1978
Erythrocyte superoxide-dismutase deficiency in Fanconi's anaemiaH Joenje, A W Eriksson, R R Frants, et al.
Clinical Genetics|July 1, 1990
Pseudoinflammatory fundus dystrophy: a follow-up studyA W Eriksson, E A Suvanto, R R Frants, et al.
Pageof 29