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J Boue

Showing results (21-30 of 27) with videos related to

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Clinical Genetics|February 1, 1989
Genetic heterogeneity between two clinical forms of cystic fibrosis evidenced by familial analysis and linked DNA probesE Mornet, B Simon-Bouy, J L Serre, et al.
Prenatal Diagnosis|July 1, 1989
Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probesM Raux-Demay, E Mornet, J Boue, et al.
Human Genetics|August 1, 1986
First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determinationE Mornet, J Boue, M Raux-Demay, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1988
Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia by simultaneous radioimmunoassay of 21-deoxycortisol and 17-hydroxyprogesterone in amniotic fluidB Gueux, J Fiet, P Couillin, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Collaborative study of the molecular epidemiology of Tay-Sachs disease in EuropeS Akli, J Boue, K Sandhoff, et al.
British Journal of Pharmacology|October 10, 2014
Protective effects of n-6 fatty acids-enriched diet on intestinal ischaemia/reperfusion injury involve lipoxin A4 and its receptorT Gobbetti, S Ducheix, P le Faouder, et al.
Nature|July 3, 1986
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophyL M Kunkel, J F Hejtmancik, C T Caskey, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Clinical Genetics|February 1, 1989
Genetic heterogeneity between two clinical forms of cystic fibrosis evidenced by familial analysis and linked DNA probesE Mornet, B Simon-Bouy, J L Serre, et al.
Prenatal Diagnosis|July 1, 1989
Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probesM Raux-Demay, E Mornet, J Boue, et al.
Human Genetics|August 1, 1986
First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determinationE Mornet, J Boue, M Raux-Demay, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1988
Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia by simultaneous radioimmunoassay of 21-deoxycortisol and 17-hydroxyprogesterone in amniotic fluidB Gueux, J Fiet, P Couillin, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Collaborative study of the molecular epidemiology of Tay-Sachs disease in EuropeS Akli, J Boue, K Sandhoff, et al.
British Journal of Pharmacology|October 10, 2014
Protective effects of n-6 fatty acids-enriched diet on intestinal ischaemia/reperfusion injury involve lipoxin A4 and its receptorT Gobbetti, S Ducheix, P le Faouder, et al.
Nature|July 3, 1986
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophyL M Kunkel, J F Hejtmancik, C T Caskey, et al.
Pageof 3