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D Vidaud

Showing results (51-60 of 70) with videos related to

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Cancer Genetics|January 25, 2025
Hepatoblastoma in a patient with neurofibromatosis type 1: A case reportA Praga, T Z Hirsch, D Vidaud, et al.
Clinical Chemistry|September 7, 2000
Prenatal detection by real-time quantitative PCR and characterization of a new CFTR deletion, 3600+15kbdel5.3kb (or CFTRdele19)B Costes, E Girodon, D Vidaud, et al.
Clinical Genetics|December 8, 1998
Detection of more than 91% cystic fibrosis mutations in a sample of the population from Reunion Island and identification of two novel mutations (A309G, S1255L) and one novel polymorphism (L49L)F Cartault, J Steffann, D Vidaud, et al.
American Journal of Human Genetics|March 28, 2003
Elevated risk for MPNST in NF1 microdeletion patientsT De Raedt, H Brems, P Wolkenstein, et al.
Blood|August 15, 2000
Somatic mosaicism and compound heterozygosity in female hemophilia BJ M Costa, D Vidaud, I Laurendeau, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Haemophilia B due to a de novo insertion of a human-specific Alu subfamily member within the coding region of the factor IX geneD Vidaud, M Vidaud, B R Bahnak, et al.
The Journal of Biological Chemistry|November 5, 1990
Important role of arginine 129 in heparin-binding site of antithrombin III. Identification of a novel mutation arginine 129 to glutamineS Gandrille, M Aiach, D A Lane, et al.
Cell Death and Differentiation|March 24, 2007
Positive regulation of apoptosis by HCA66, a new Apaf-1 interacting protein, and its putative role in the physiopathology of NF1 microdeletion syndrome patientsV Piddubnyak, P Rigou, L Michel, et al.
British Journal of Haematology|August 1, 1993
Detection of a molecular defect in 40 of 44 patients with haemophilia B by PCR and denaturing gradient gel electrophoresisM Tartary, D Vidaud, Y Piao, et al.
Annales De Genetique|January 1, 1997
Familial aggregation of malignant melanoma/dysplastic naevi and tumours of the nervous system: an original syndrome of tumour pronenessM Bahuau, D Vidaud, M Kujas, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Cancer Genetics|January 25, 2025
Hepatoblastoma in a patient with neurofibromatosis type 1: A case reportA Praga, T Z Hirsch, D Vidaud, et al.
Clinical Chemistry|September 7, 2000
Prenatal detection by real-time quantitative PCR and characterization of a new CFTR deletion, 3600+15kbdel5.3kb (or CFTRdele19)B Costes, E Girodon, D Vidaud, et al.
Clinical Genetics|December 8, 1998
Detection of more than 91% cystic fibrosis mutations in a sample of the population from Reunion Island and identification of two novel mutations (A309G, S1255L) and one novel polymorphism (L49L)F Cartault, J Steffann, D Vidaud, et al.
American Journal of Human Genetics|March 28, 2003
Elevated risk for MPNST in NF1 microdeletion patientsT De Raedt, H Brems, P Wolkenstein, et al.
Blood|August 15, 2000
Somatic mosaicism and compound heterozygosity in female hemophilia BJ M Costa, D Vidaud, I Laurendeau, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Haemophilia B due to a de novo insertion of a human-specific Alu subfamily member within the coding region of the factor IX geneD Vidaud, M Vidaud, B R Bahnak, et al.
The Journal of Biological Chemistry|November 5, 1990
Important role of arginine 129 in heparin-binding site of antithrombin III. Identification of a novel mutation arginine 129 to glutamineS Gandrille, M Aiach, D A Lane, et al.
Cell Death and Differentiation|March 24, 2007
Positive regulation of apoptosis by HCA66, a new Apaf-1 interacting protein, and its putative role in the physiopathology of NF1 microdeletion syndrome patientsV Piddubnyak, P Rigou, L Michel, et al.
British Journal of Haematology|August 1, 1993
Detection of a molecular defect in 40 of 44 patients with haemophilia B by PCR and denaturing gradient gel electrophoresisM Tartary, D Vidaud, Y Piao, et al.
Annales De Genetique|January 1, 1997
Familial aggregation of malignant melanoma/dysplastic naevi and tumours of the nervous system: an original syndrome of tumour pronenessM Bahuau, D Vidaud, M Kujas, et al.
Pageof 7