L Foubert|P Benlian|J L de Gennes - JoVE Visualize

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Bulletin De L'Academie Nationale De Medecine|March 1, 1994

[Molecular genetics and lipoprotein lipase deficiency]L Foubert, P Benlian, J L de Gennes

The New England Journal of Medicine|September 19, 1996

Premature atherosclerosis in patients with familial chylomicronemia caused by mutations in the lipoprotein lipase geneP Benlian, J L De Gennes, L Foubert, et al.

American Journal of Human Genetics|August 1, 1996

Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiencyP Benlian, L Foubert, E Gagné, et al.

Bulletin De L'Academie Nationale De Medecine|March 1, 1994

[Molecular genetics in pure primary hypercholesterolemia]P Benlian, F Dairou, J L de Gennes

Human Mutation|January 1, 1997

A single Ser259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestryL Foubert, T Bruin, J L De Gennes, et al.

Journal of Medical Genetics|August 1, 1997

Assessment of French patients with LPL deficiency for French Canadian mutationsL Foubert, J L De Gennes, J P Lagarde, et al.

Annales D'Endocrinologie|September 29, 2007

[Blood screening of glucose and lipid disorders as coronary atherosclerosis risks factors in French adolescents 16 to 19-20 years old]J-L de Gennes, P Benlian, C Dreux, et al.

Presse Medicale (Paris, France : 1983)|February 10, 1996

[Lipoprotein lipase: a multifunctional enzyme in lipoprotein metabolism]L Foubert, P Benlian, G Turpin

Journal of Lipid Research|February 1, 1995

Homozygous deletion of exon 9 causes lipoprotein lipase deficiency: possible intron-Alu recombinationP Benlian, J Etienne, J L de Gennes, et al.

Human Mutation|January 1, 1994

Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestriesY Ma, M S Liu, D Chitayat, et al.

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Showing results (1-10 of 174) with videos related to

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Pageof 18

Bulletin De L'Academie Nationale De Medecine|March 1, 1994

[Molecular genetics and lipoprotein lipase deficiency]L Foubert, P Benlian, J L de Gennes

The New England Journal of Medicine|September 19, 1996

Premature atherosclerosis in patients with familial chylomicronemia caused by mutations in the lipoprotein lipase geneP Benlian, J L De Gennes, L Foubert, et al.

American Journal of Human Genetics|August 1, 1996

Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiencyP Benlian, L Foubert, E Gagné, et al.

Bulletin De L'Academie Nationale De Medecine|March 1, 1994

[Molecular genetics in pure primary hypercholesterolemia]P Benlian, F Dairou, J L de Gennes

Human Mutation|January 1, 1997

A single Ser259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestryL Foubert, T Bruin, J L De Gennes, et al.

Journal of Medical Genetics|August 1, 1997

Assessment of French patients with LPL deficiency for French Canadian mutationsL Foubert, J L De Gennes, J P Lagarde, et al.

Annales D'Endocrinologie|September 29, 2007

[Blood screening of glucose and lipid disorders as coronary atherosclerosis risks factors in French adolescents 16 to 19-20 years old]J-L de Gennes, P Benlian, C Dreux, et al.

Presse Medicale (Paris, France : 1983)|February 10, 1996

[Lipoprotein lipase: a multifunctional enzyme in lipoprotein metabolism]L Foubert, P Benlian, G Turpin

Journal of Lipid Research|February 1, 1995

Homozygous deletion of exon 9 causes lipoprotein lipase deficiency: possible intron-Alu recombinationP Benlian, J Etienne, J L de Gennes, et al.

Human Mutation|January 1, 1994

Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestriesY Ma, M S Liu, D Chitayat, et al.

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