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Claude Houdayer

Showing results (11-20 of 113) with videos related to

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Genetic Testing|September 7, 2002
Simple fluorescent PCR assay for discriminating FRAXA fully mutated females from normal homozygotesClaude Houdayer, Julie Lourdaux, Thierry Billette de Villemeur, et al.
Prenatal Diagnosis|September 10, 2011
Mosaicism in clinical practice exemplified by prenatal diagnosis in retinoblastomaLaurent Castéra, Marion Gauthier-Villars, Catherine Dehainault, et al.
Familial Cancer|January 8, 2022
Detecting inversions in routine molecular diagnosis in MMR genesEdwige Kasper, Sophie Coutant, Sandrine Manase, et al.
American Journal of Medical Genetics. Part A|March 25, 2004
Mutation of SFTPC in infantile pulmonary alveolar proteinosis with or without fibrosing lung diseaseMohammed Tredano, Matthias Griese, Frank Brasch, et al.
Familial Cancer|August 19, 2017
Sporadic endometrial adenocarcinoma with MMR deficiency due to biallelic MSH2 somatic mutationsBruno Buecher, Antoine De Pauw, Louis Bazire, et al.
Investigative Ophthalmology & Visual Science|September 23, 2016
Combination of Carboplatin and Bevacizumab Is an Efficient Therapeutic Approach in Retinoblastoma Patient-Derived XenograftsFranck Assayag, André Nicolas, Sophie Vacher, et al.
Cancers|April 13, 2023
Disequilibrium between <i>BRCA1</i> and <i>BRCA2</i> Circular and Messenger RNAs Plays a Role in Breast CancerCorentin Levacher, Mathieu Viennot, Aurélie Drouet, et al.
Pediatric Blood & Cancer|February 23, 2018
Mutiple DICER1-related lesions associated with a germline deep intronic mutationFlorian Verrier, Catherine Dubois d'Enghien, Marion Gauthier-Villars, et al.
Human Mutation|November 11, 2006
Genotype-phenotype correlations in hereditary familial retinoblastomaMelissa Taylor, Catherine Dehainault, Laurence Desjardins, et al.
Familial Cancer|February 7, 2025
New RPS20 gene variant in colorectal cancer diagnosis: insight from a large series of patientsJulie Amiot, Lara Gubeljak, Agathe Fontaine, et al.
Pageof 12

Showing results (11-20 of 113) with videos related to

Sort By:
Pageof 12
Genetic Testing|September 7, 2002
Simple fluorescent PCR assay for discriminating FRAXA fully mutated females from normal homozygotesClaude Houdayer, Julie Lourdaux, Thierry Billette de Villemeur, et al.
Prenatal Diagnosis|September 10, 2011
Mosaicism in clinical practice exemplified by prenatal diagnosis in retinoblastomaLaurent Castéra, Marion Gauthier-Villars, Catherine Dehainault, et al.
Familial Cancer|January 8, 2022
Detecting inversions in routine molecular diagnosis in MMR genesEdwige Kasper, Sophie Coutant, Sandrine Manase, et al.
American Journal of Medical Genetics. Part A|March 25, 2004
Mutation of SFTPC in infantile pulmonary alveolar proteinosis with or without fibrosing lung diseaseMohammed Tredano, Matthias Griese, Frank Brasch, et al.
Familial Cancer|August 19, 2017
Sporadic endometrial adenocarcinoma with MMR deficiency due to biallelic MSH2 somatic mutationsBruno Buecher, Antoine De Pauw, Louis Bazire, et al.
Investigative Ophthalmology & Visual Science|September 23, 2016
Combination of Carboplatin and Bevacizumab Is an Efficient Therapeutic Approach in Retinoblastoma Patient-Derived XenograftsFranck Assayag, André Nicolas, Sophie Vacher, et al.
Cancers|April 13, 2023
Disequilibrium between <i>BRCA1</i> and <i>BRCA2</i> Circular and Messenger RNAs Plays a Role in Breast CancerCorentin Levacher, Mathieu Viennot, Aurélie Drouet, et al.
Pediatric Blood & Cancer|February 23, 2018
Mutiple DICER1-related lesions associated with a germline deep intronic mutationFlorian Verrier, Catherine Dubois d'Enghien, Marion Gauthier-Villars, et al.
Human Mutation|November 11, 2006
Genotype-phenotype correlations in hereditary familial retinoblastomaMelissa Taylor, Catherine Dehainault, Laurence Desjardins, et al.
Familial Cancer|February 7, 2025
New RPS20 gene variant in colorectal cancer diagnosis: insight from a large series of patientsJulie Amiot, Lara Gubeljak, Agathe Fontaine, et al.
Pageof 12