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R R Frants

Showing results (31-40 of 282) with videos related to

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Human Genetics|January 1, 1985
The alpha 1 antitrypsin variant PI WFINNEYTOWN in a family of Caucasian originE C Klasen, C D Laros, A Bröcker-Vriends, et al.
Lancet (London, England)|July 5, 1975
Letter: Superoxide dismutase in Down syndromeR R Frants, A W Eriksson, P H Jongbloet, et al.
Trends in Pharmacological Sciences|June 5, 1998
P/Q-type Ca2+ channel defects in migraine, ataxia and epilepsyR A Ophoff, G M Terwindt, R R Frants, et al.
Thrombosis and Haemostasis|February 23, 1981
Recent investigations of the first bleeder family in Aland (Finland) described by von WillebrandD Nyman, A W Eriksson, M Blombäck, et al.
Clinical Neurology and Neurosurgery|June 1, 1993
Hereditary spastic paraparesis. Clinical and genetic data from a large Dutch familyR P Bruyn, J van Deutekom, R R Frants, et al.
Human Genetics|May 1, 1992
Protease inhibitor (Pi) locus, fertility and twinningD I Boomsma, R R Frants, R A Bank, et al.
Muscle & Nerve|February 1, 1994
Dominant congenital benign spinal muscular atrophyC J Frijns, J Van Deutekom, R R Frants, et al.
Histology and Histopathology|August 5, 1998
Genetics and pathology of voltage-gated Ca2+ channelsR A Ophoff, G M Terwindt, M D Ferrari, et al.
The Journal of Investigative Dermatology. Symposium Proceedings|October 28, 1999
Familial melanoma; CDKN2A and beyondN A Gruis, P A van der Velden, W Bergman, et al.
Muscle & Nerve. Supplement|January 1, 1995
Early onset facioscapulohumeral muscular dystrophyO F Brouwer, G W Padberg, E Bakker, et al.
Pageof 29

Showing results (31-40 of 282) with videos related to

Sort By:
Pageof 29
Human Genetics|January 1, 1985
The alpha 1 antitrypsin variant PI WFINNEYTOWN in a family of Caucasian originE C Klasen, C D Laros, A Bröcker-Vriends, et al.
Lancet (London, England)|July 5, 1975
Letter: Superoxide dismutase in Down syndromeR R Frants, A W Eriksson, P H Jongbloet, et al.
Trends in Pharmacological Sciences|June 5, 1998
P/Q-type Ca2+ channel defects in migraine, ataxia and epilepsyR A Ophoff, G M Terwindt, R R Frants, et al.
Thrombosis and Haemostasis|February 23, 1981
Recent investigations of the first bleeder family in Aland (Finland) described by von WillebrandD Nyman, A W Eriksson, M Blombäck, et al.
Clinical Neurology and Neurosurgery|June 1, 1993
Hereditary spastic paraparesis. Clinical and genetic data from a large Dutch familyR P Bruyn, J van Deutekom, R R Frants, et al.
Human Genetics|May 1, 1992
Protease inhibitor (Pi) locus, fertility and twinningD I Boomsma, R R Frants, R A Bank, et al.
Muscle & Nerve|February 1, 1994
Dominant congenital benign spinal muscular atrophyC J Frijns, J Van Deutekom, R R Frants, et al.
Histology and Histopathology|August 5, 1998
Genetics and pathology of voltage-gated Ca2+ channelsR A Ophoff, G M Terwindt, M D Ferrari, et al.
The Journal of Investigative Dermatology. Symposium Proceedings|October 28, 1999
Familial melanoma; CDKN2A and beyondN A Gruis, P A van der Velden, W Bergman, et al.
Muscle & Nerve. Supplement|January 1, 1995
Early onset facioscapulohumeral muscular dystrophyO F Brouwer, G W Padberg, E Bakker, et al.
Pageof 29