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Marion Gauthier

Showing results (41-50 of 108) with videos related to

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Journal of the National Cancer Institute|November 6, 2010
MDM2 as a modifier gene in retinoblastomaLaurent Castéra, Audrey Sabbagh, Catherine Dehainault, et al.
Human Molecular Genetics|May 27, 2014
The survival gene MED4 explains low penetrance retinoblastoma in patients with large RB1 deletionCatherine Dehainault, Alexandra Garancher, Laurent Castéra, et al.
Human Mutation|December 2, 2010
EMMA, a cost- and time-effective diagnostic method for simultaneous detection of point mutations and large-scale genomic rearrangements: application to BRCA1 and BRCA2 in 1,525 patientsVirginie Caux-Moncoutier, Laurent Castéra, Carole Tirapo, et al.
European Journal of Medical Genetics|July 22, 2018
Correlation between RB1germline mutations and second primary malignancies in hereditary retinoblastoma patients treated with external beam radiotherapyAmélie Chaussade, Gaël Millot, Constance Wells, et al.
Human Mutation|February 13, 2004
Characterisation of a 161 kb deletion extending from the NBR1 to the BRCA1 genes in a French breast-ovarian cancer familySophie Gad, Ivan Bièche, Michel Barrois, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 6, 2013
Results of a multicenter prospective study on the postoperative treatment of unilateral retinoblastoma after primary enucleationIsabelle Aerts, Xavier Sastre-Garau, Alexia Savignoni, et al.
JAMA Ophthalmology|June 20, 2020
Association Between Genotype and Phenotype in Consecutive Unrelated Individuals With RetinoblastomaFlore Salviat, Marion Gauthier-Villars, Matthieu Carton, et al.
Bulletin Du Cancer|January 23, 2025
Bone sarcomas and cancer predisposition syndromesCamille Tlemsani, Gaëlle Bougeard, Marion Gauthier-Villars, et al.
Journal of Pediatric Hematology/Oncology|February 17, 2025
PHOX2B -associated Congenital Central Hypoventilation Syndrome Revealed Upon Treatment With Dinutuximab-betaAlix Chupin, Benjamin Dudoignon, Nathalie Couque, et al.
The Journal of Molecular Diagnostics : JMD|October 17, 2021
Highly Sensitive Detection Method of Retinoblastoma Genetic Predisposition and BiomarkersJessica Le Gall, Catherine Dehainault, Camille Benoist, et al.
Pageof 11

Showing results (41-50 of 108) with videos related to

Sort By:
Pageof 11
Journal of the National Cancer Institute|November 6, 2010
MDM2 as a modifier gene in retinoblastomaLaurent Castéra, Audrey Sabbagh, Catherine Dehainault, et al.
Human Molecular Genetics|May 27, 2014
The survival gene MED4 explains low penetrance retinoblastoma in patients with large RB1 deletionCatherine Dehainault, Alexandra Garancher, Laurent Castéra, et al.
Human Mutation|December 2, 2010
EMMA, a cost- and time-effective diagnostic method for simultaneous detection of point mutations and large-scale genomic rearrangements: application to BRCA1 and BRCA2 in 1,525 patientsVirginie Caux-Moncoutier, Laurent Castéra, Carole Tirapo, et al.
European Journal of Medical Genetics|July 22, 2018
Correlation between RB1germline mutations and second primary malignancies in hereditary retinoblastoma patients treated with external beam radiotherapyAmélie Chaussade, Gaël Millot, Constance Wells, et al.
Human Mutation|February 13, 2004
Characterisation of a 161 kb deletion extending from the NBR1 to the BRCA1 genes in a French breast-ovarian cancer familySophie Gad, Ivan Bièche, Michel Barrois, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 6, 2013
Results of a multicenter prospective study on the postoperative treatment of unilateral retinoblastoma after primary enucleationIsabelle Aerts, Xavier Sastre-Garau, Alexia Savignoni, et al.
JAMA Ophthalmology|June 20, 2020
Association Between Genotype and Phenotype in Consecutive Unrelated Individuals With RetinoblastomaFlore Salviat, Marion Gauthier-Villars, Matthieu Carton, et al.
Bulletin Du Cancer|January 23, 2025
Bone sarcomas and cancer predisposition syndromesCamille Tlemsani, Gaëlle Bougeard, Marion Gauthier-Villars, et al.
Journal of Pediatric Hematology/Oncology|February 17, 2025
PHOX2B -associated Congenital Central Hypoventilation Syndrome Revealed Upon Treatment With Dinutuximab-betaAlix Chupin, Benjamin Dudoignon, Nathalie Couque, et al.
The Journal of Molecular Diagnostics : JMD|October 17, 2021
Highly Sensitive Detection Method of Retinoblastoma Genetic Predisposition and BiomarkersJessica Le Gall, Catherine Dehainault, Camille Benoist, et al.
Pageof 11