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T Frebourg

Showing results (51-60 of 103) with videos related to

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Genes, Chromosomes & Cancer|January 9, 2008
Non-Hodgkin lymphoma related to hereditary nonpolyposis colorectal cancer in a patient with a novel heterozygous complex deletion in the MSH2 geneM Pineda, E Castellsagué, E Musulén, et al.
Blood|August 15, 1997
The A20210 allele of the prothrombin gene is not frequently associated with the factor V Arg 506 to Gln mutation in thrombophilic familiesM Alhenc-Gelas, V Le Cam-Duchez, J Emmerich, et al.
Journal of Medical Genetics|February 4, 2005
Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformationsC Le Caignec, M Boceno, P Saugier-Veber, et al.
Journal of Medical Genetics|July 22, 2005
Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an updateG Raux, L Guyant-Maréchal, C Martin, et al.
Clinical Genetics|March 30, 2011
Frequent mutation in North African patients with MUTYH-associated polyposisJ H Lefevre, C Colas, F Coulet, et al.
Neurology|December 3, 2008
Intrafamilial diversity of phenotype associated with app duplicationI Guyant-Marechal, E Berger, A Laquerrière, et al.
American Journal of Human Genetics|March 1, 1995
Germ-line p53 mutations in 15 families with Li-Fraumeni syndromeT Frebourg, N Barbier, Y X Yan, et al.
Annales De Dermatologie Et De Venereologie|March 16, 2010
[Intra- and interfamilial phenotype variation in Birt-Hogg-Dubé syndrome: Consequences for therapy]M Steff, A Bourillon, T Frebourg, et al.
Human Molecular Genetics|June 17, 1999
Presenilins interact with Rab11, a small GTPase involved in the regulation of vesicular transportC Dumanchin, C Czech, D Campion, et al.
Journal of Medical Genetics|August 27, 1998
De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study GroupC Dumanchin, A Brice, D Campion, et al.
Pageof 11

Showing results (51-60 of 103) with videos related to

Sort By:
Pageof 11
Genes, Chromosomes & Cancer|January 9, 2008
Non-Hodgkin lymphoma related to hereditary nonpolyposis colorectal cancer in a patient with a novel heterozygous complex deletion in the MSH2 geneM Pineda, E Castellsagué, E Musulén, et al.
Blood|August 15, 1997
The A20210 allele of the prothrombin gene is not frequently associated with the factor V Arg 506 to Gln mutation in thrombophilic familiesM Alhenc-Gelas, V Le Cam-Duchez, J Emmerich, et al.
Journal of Medical Genetics|February 4, 2005
Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformationsC Le Caignec, M Boceno, P Saugier-Veber, et al.
Journal of Medical Genetics|July 22, 2005
Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an updateG Raux, L Guyant-Maréchal, C Martin, et al.
Clinical Genetics|March 30, 2011
Frequent mutation in North African patients with MUTYH-associated polyposisJ H Lefevre, C Colas, F Coulet, et al.
Neurology|December 3, 2008
Intrafamilial diversity of phenotype associated with app duplicationI Guyant-Marechal, E Berger, A Laquerrière, et al.
American Journal of Human Genetics|March 1, 1995
Germ-line p53 mutations in 15 families with Li-Fraumeni syndromeT Frebourg, N Barbier, Y X Yan, et al.
Annales De Dermatologie Et De Venereologie|March 16, 2010
[Intra- and interfamilial phenotype variation in Birt-Hogg-Dubé syndrome: Consequences for therapy]M Steff, A Bourillon, T Frebourg, et al.
Human Molecular Genetics|June 17, 1999
Presenilins interact with Rab11, a small GTPase involved in the regulation of vesicular transportC Dumanchin, C Czech, D Campion, et al.
Journal of Medical Genetics|August 27, 1998
De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study GroupC Dumanchin, A Brice, D Campion, et al.
Pageof 11