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J Feingold

Showing results (71-80 of 307) with videos related to

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Archives Francaises De Pediatrie|October 1, 1970
[Results of an investigation on the birth weight and the weight of the placenta]J Feingold, J Frézal, M L Briard-Guillemot
Revue Neurologique|May 24, 2015
Guidelines for presymptomatic testing for Huntington's disease: past, present and future in FranceS Clément, M Gargiulo, J Feingold, et al.
Monographs in Human Genetics|January 1, 1978
Idiopathic haemochromatosis diabetes: assessment of serum iron and transferin saturation in high and low risk populations for diabetes mellitusR Saddi, J Feingold, R Fagard, et al.
American Journal of Medical Genetics|January 1, 1994
Parental consanguinity as a cause of increased incidence of birth defects in a study of 131,760 consecutive birthsC Stoll, Y Alembik, B Dott, et al.
Journal of Molecular Biology|January 5, 1986
Transcription initiation in vitro and in vivo at a highly conserved promoter within a 16 S ribosomal RNA geneK Amemiya, V Bellofatto, L Shapiro, et al.
European Psychiatry : the Journal of the Association of European Psychiatrists|August 25, 2009
A one year prevalence study of schizophrenia on Reunion IslandM Jay, P Gorwood, J Feingold, et al.
Biochimie|January 1, 1974
Iron stimulation of ferritin biosynthesis. I. Localization of the iron effectR Saddi, R Fagard, J Feingold, et al.
BMJ (Clinical Research Ed.)|December 14, 1999
Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort studyM Gabolde, M Guilloud-Bataille, J Feingold, et al.
Journal of Medical Genetics|December 1, 1976
Infantile cystinosis in France: genetics, incidence, geographic distributionE Bois, J Feingold, P Frenay, et al.
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]|January 1, 1978
Desferrioxamine utilisation for the quantitation of iron excess. Study of 24 patients having idiopathic haemochromatosisR Saddi, J Feingold, C H Degrese, et al.
Pageof 31

Showing results (71-80 of 307) with videos related to

Sort By:
Pageof 31
Archives Francaises De Pediatrie|October 1, 1970
[Results of an investigation on the birth weight and the weight of the placenta]J Feingold, J Frézal, M L Briard-Guillemot
Revue Neurologique|May 24, 2015
Guidelines for presymptomatic testing for Huntington's disease: past, present and future in FranceS Clément, M Gargiulo, J Feingold, et al.
Monographs in Human Genetics|January 1, 1978
Idiopathic haemochromatosis diabetes: assessment of serum iron and transferin saturation in high and low risk populations for diabetes mellitusR Saddi, J Feingold, R Fagard, et al.
American Journal of Medical Genetics|January 1, 1994
Parental consanguinity as a cause of increased incidence of birth defects in a study of 131,760 consecutive birthsC Stoll, Y Alembik, B Dott, et al.
Journal of Molecular Biology|January 5, 1986
Transcription initiation in vitro and in vivo at a highly conserved promoter within a 16 S ribosomal RNA geneK Amemiya, V Bellofatto, L Shapiro, et al.
European Psychiatry : the Journal of the Association of European Psychiatrists|August 25, 2009
A one year prevalence study of schizophrenia on Reunion IslandM Jay, P Gorwood, J Feingold, et al.
Biochimie|January 1, 1974
Iron stimulation of ferritin biosynthesis. I. Localization of the iron effectR Saddi, R Fagard, J Feingold, et al.
BMJ (Clinical Research Ed.)|December 14, 1999
Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort studyM Gabolde, M Guilloud-Bataille, J Feingold, et al.
Journal of Medical Genetics|December 1, 1976
Infantile cystinosis in France: genetics, incidence, geographic distributionE Bois, J Feingold, P Frenay, et al.
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]|January 1, 1978
Desferrioxamine utilisation for the quantitation of iron excess. Study of 24 patients having idiopathic haemochromatosisR Saddi, J Feingold, C H Degrese, et al.
Pageof 31