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Archives of Neurology|July 16, 2008
Clinical and molecular findings of ataxia with oculomotor apraxia type 2 in 4 familiesMathieu Anheim, Marie-Celine Fleury, Jerome Franques, et al.
Genes, Chromosomes & Cancer|April 22, 2004
Functional consequences of ATM sequence variants for chromosomal radiosensitivitySara Gutiérrez-Enríquez, Marie Fernet, Thilo Dörk, et al.
Cancer Research|June 5, 2007
X inactive-specific transcript RNA coating and genetic instability of the X chromosome in BRCA1 breast tumorsAnne Vincent-Salomon, Carine Ganem-Elbaz, Elodie Manié, et al.
Journal of Medical Genetics|December 18, 2013
A new scoring system in cancer genetics: application to criteria for BRCA1 and BRCA2 mutation screeningBernard Bonaïti, Flora Alarcon, Nadine Andrieu, et al.
Human Mutation|September 17, 2011
Assessment of human Nter and Cter BRCA1 mutations using growth and localization assays in yeastGaël A Millot, Adeline Berger, Vincent Lejour, et al.
Proteomics. Clinical Applications|December 8, 2010
Proteomic analysis of BRCA1-depleted cell line reveals a putative role for replication protein A2 up-regulation in BRCA1 breast tumor developmentJulien Bouley, Cédric Pionneau, Justine Varinot, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2017
Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemiaMassimo Bogliolo, Dominique Bluteau, James Lespinasse, et al.
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