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D Vidaud

Showing results (61-70 of 70) with videos related to

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American Journal of Medical Genetics|December 18, 1996
Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis associationM Bahuau, W Flintoff, B Assouline, et al.
Human Genetics|April 1, 1993
Nucleotide substitutions at the -6 position in the promoter region of the factor IX gene result in different severity of hemophilia B Leyden: consequences for genetic counselingD Vidaud, M Tartary, J M Costa, et al.
American Journal of Medical Genetics|February 25, 1998
Novel recurrent nonsense mutation causing neurofibromatosis type 1 (NF1) in a family segregating both NF1 and Noonan syndromeM Bahuau, C Houdayer, B Assouline, et al.
The EMBO Journal|November 1, 1991
Towards a transgenic mouse model of sickle cell disease: hemoglobin SADM Trudel, N Saadane, M C Garel, et al.
Human Mutation|September 12, 2000
NF1 gene analysis focused on CpG-rich exons in a cohort of 93 patients with neurofibromatosis type 1E Girodon-Boulandet, J Pantel, C Cazeneuve, et al.
Journal of Medical Genetics|March 11, 2000
Tandem duplication within the neurofibromatosis type 1 gene (NF1) and reciprocal t(15;16)(q26.3;q12.1) translocation in familial association of NF1 with intestinal neuronal dysplasia type B (IND B)M Bahuau, I Laurendeau, A Pelet, et al.
Gut|October 23, 2003
Liver fibrosis is not associated with steatosis but with necroinflammation in French patients with chronic hepatitis CT Asselah, N Boyer, M-C Guimont, et al.
Cancer Research|June 11, 1998
Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumorsM Bahuau, D Vidaud, R B Jenkins, et al.
Journal of Medical Genetics|April 16, 2009
SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotypeE Pasmant, A Sabbagh, N Hanna, et al.
Oncogene|January 29, 2014
SPRED1, a RAS MAPK pathway inhibitor that causes Legius syndrome, is a tumour suppressor downregulated in paediatric acute myeloblastic leukaemiaE Pasmant, B Gilbert-Dussardier, A Petit, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
American Journal of Medical Genetics|December 18, 1996
Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis associationM Bahuau, W Flintoff, B Assouline, et al.
Human Genetics|April 1, 1993
Nucleotide substitutions at the -6 position in the promoter region of the factor IX gene result in different severity of hemophilia B Leyden: consequences for genetic counselingD Vidaud, M Tartary, J M Costa, et al.
American Journal of Medical Genetics|February 25, 1998
Novel recurrent nonsense mutation causing neurofibromatosis type 1 (NF1) in a family segregating both NF1 and Noonan syndromeM Bahuau, C Houdayer, B Assouline, et al.
The EMBO Journal|November 1, 1991
Towards a transgenic mouse model of sickle cell disease: hemoglobin SADM Trudel, N Saadane, M C Garel, et al.
Human Mutation|September 12, 2000
NF1 gene analysis focused on CpG-rich exons in a cohort of 93 patients with neurofibromatosis type 1E Girodon-Boulandet, J Pantel, C Cazeneuve, et al.
Journal of Medical Genetics|March 11, 2000
Tandem duplication within the neurofibromatosis type 1 gene (NF1) and reciprocal t(15;16)(q26.3;q12.1) translocation in familial association of NF1 with intestinal neuronal dysplasia type B (IND B)M Bahuau, I Laurendeau, A Pelet, et al.
Gut|October 23, 2003
Liver fibrosis is not associated with steatosis but with necroinflammation in French patients with chronic hepatitis CT Asselah, N Boyer, M-C Guimont, et al.
Cancer Research|June 11, 1998
Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumorsM Bahuau, D Vidaud, R B Jenkins, et al.
Journal of Medical Genetics|April 16, 2009
SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotypeE Pasmant, A Sabbagh, N Hanna, et al.
Oncogene|January 29, 2014
SPRED1, a RAS MAPK pathway inhibitor that causes Legius syndrome, is a tumour suppressor downregulated in paediatric acute myeloblastic leukaemiaE Pasmant, B Gilbert-Dussardier, A Petit, et al.
Pageof 7