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Cancers|July 2, 2021
5' Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent BreakpointsSandrine M Caputo, Dominique Telly, Adrien Briaux, et al.Forensic Science International|April 20, 2001
Online reference database of European Y-chromosomal short tandem repeat (STR) haplotypesL Roewer, M Krawczak, S Willuweit, et al.Forensic Science International. Genetics|December 17, 2008
2006 GEP-ISFG collaborative exercise on mtDNA: reflections about interpretation, artefacts, and DNA mixturesL Prieto, A Alonso, C Alves, et al.Human Mutation|December 9, 2021
Novel germline MET pathogenic variants in French patients with papillary renal cell carcinomas type IMolka Sebai, David Tulasne, Sandrine M Caputo, et al.Cancer Discovery|April 24, 2021
NKX3.1 Localization to Mitochondria Suppresses Prostate Cancer InitiationAlexandros Papachristodoulou, Antonio Rodriguez-Calero, Sukanya Panja, et al.Cancer Medicine|August 28, 2024
Atypical cancer risk profile in carriers of Italian founder BRCA1 variant p.His1673del: Implications for classification and clinical managementGiovanni Innella, Cristina Fortuno, Laura Caleca, et al.Human Mutation|October 13, 2005
Mutation rates at Y chromosome specific microsatellitesL Gusmão, P Sánchez-Diz, F Calafell, et al.Cancer Research|February 13, 2020
Skipping Nonsense to Maintain Function: The Paradigm of BRCA2 Exon 12Laëtitia Meulemans, Romy L S Mesman, Sandrine M Caputo, et al.Oncotarget|May 1, 2018
Full in-frame exon 3 skipping of BRCA2 confers high risk of breast and/or ovarian cancerSandrine M Caputo, Mélanie Léone, Francesca Damiola, et al.Nucleic Acids Research|May 12, 2018
Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effortRaphaël Leman, Pascaline Gaildrat, Gérald Le Gac, et al.Pageof 33