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European Journal of Cancer (Oxford, England : 1990)
|
June 16, 2021
Wilms tumour surveillance in at-risk children: Literature review and recommendations from the SIOP-Europe Host Genome Working Group and SIOP Renal Tumour Study Group
Janna A Hol, Rosalyn Jewell, Tanzina Chowdhury, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
May 28, 2015
Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers
Gaëlle Bougeard, Mariette Renaux-Petel, Jean-Michel Flaman, et al.
Clinical Genetics
|
March 28, 2023
Hereditary cancer predispositions: Comparison of multigene panel sequencing on fresh-frozen breast/ovarian tumor versus blood
Mathias Schwartz, Virginie Moncoutier, Adrien Peytral, et al.
Plos One
|
September 26, 2015
Targeted Sequencing of the Mitochondrial Genome of Women at High Risk of Breast Cancer without Detectable Mutations in BRCA1/2
Sophie Blein, Laure Barjhoux, , et al.
European Journal of Human Genetics : EJHG
|
December 20, 2017
Contribution of germline deleterious variants in the RAD51 paralogs to breast and ovarian cancers
Lisa Golmard, Laurent Castéra, Sophie Krieger, et al.
European Journal of Cancer (Oxford, England : 1990)
|
July 23, 2021
Molecular diagnosis of retinoblastoma by circulating tumor DNA analysis
Irene Jiménez, Éléonore Frouin, Mathieu Chicard, et al.
The Journal of Pathology
|
January 24, 2025
SMARCB1-deficient malignant melanocytic uveal tumours: a new neural crest-derived tumour entity with SMARCB1-related germline predisposition
Joanna Cyrta, Julien Masliah-Planchon, Owen Hoare, et al.
Journal of Medical Genetics
|
March 30, 2021
Testicular Sertoli cell tumour and potentially testicular Leydig cell tumour are features of <i>DICER1</i> syndrome
Lisa Golmard, Lauren M Vasta, Valérie Duflos, et al.
Breast Cancer Research : BCR
|
July 6, 2012
Variation in breast cancer risk associated with factors related to pregnancies according to truncating mutation location, in the French National BRCA1 and BRCA2 mutations carrier cohort (GENEPSO)
Julie Lecarpentier, Catherine Noguès, Emmanuelle Mouret-Fourme, et al.
Breast Cancer Research and Treatment
|
November 14, 2015
Mutation analysis of PALB2 gene in French breast cancer families
Francesca Damiola, Inès Schultz, Laure Barjhoux, et al.
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Search research articles
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Showing results (61-70 of 108) with videos related to
Sort By:
Page
of 11
European Journal of Cancer (Oxford, England : 1990)
|
June 16, 2021
Wilms tumour surveillance in at-risk children: Literature review and recommendations from the SIOP-Europe Host Genome Working Group and SIOP Renal Tumour Study Group
Janna A Hol, Rosalyn Jewell, Tanzina Chowdhury, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
May 28, 2015
Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers
Gaëlle Bougeard, Mariette Renaux-Petel, Jean-Michel Flaman, et al.
Clinical Genetics
|
March 28, 2023
Hereditary cancer predispositions: Comparison of multigene panel sequencing on fresh-frozen breast/ovarian tumor versus blood
Mathias Schwartz, Virginie Moncoutier, Adrien Peytral, et al.
Plos One
|
September 26, 2015
Targeted Sequencing of the Mitochondrial Genome of Women at High Risk of Breast Cancer without Detectable Mutations in BRCA1/2
Sophie Blein, Laure Barjhoux, , et al.
European Journal of Human Genetics : EJHG
|
December 20, 2017
Contribution of germline deleterious variants in the RAD51 paralogs to breast and ovarian cancers
Lisa Golmard, Laurent Castéra, Sophie Krieger, et al.
European Journal of Cancer (Oxford, England : 1990)
|
July 23, 2021
Molecular diagnosis of retinoblastoma by circulating tumor DNA analysis
Irene Jiménez, Éléonore Frouin, Mathieu Chicard, et al.
The Journal of Pathology
|
January 24, 2025
SMARCB1-deficient malignant melanocytic uveal tumours: a new neural crest-derived tumour entity with SMARCB1-related germline predisposition
Joanna Cyrta, Julien Masliah-Planchon, Owen Hoare, et al.
Journal of Medical Genetics
|
March 30, 2021
Testicular Sertoli cell tumour and potentially testicular Leydig cell tumour are features of <i>DICER1</i> syndrome
Lisa Golmard, Lauren M Vasta, Valérie Duflos, et al.
Breast Cancer Research : BCR
|
July 6, 2012
Variation in breast cancer risk associated with factors related to pregnancies according to truncating mutation location, in the French National BRCA1 and BRCA2 mutations carrier cohort (GENEPSO)
Julie Lecarpentier, Catherine Noguès, Emmanuelle Mouret-Fourme, et al.
Breast Cancer Research and Treatment
|
November 14, 2015
Mutation analysis of PALB2 gene in French breast cancer families
Francesca Damiola, Inès Schultz, Laure Barjhoux, et al.
Page
of 11