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3 documents
- Roseline Vibert, Jasmine Hasnaoui, Alexandre Perrier, Alexandra Lefebvre, Chrystelle Colas, et al.. Lynch syndrome: influence of additional susceptibility variants on cancer risk. European Journal of Human Genetics, 2023, 15 (1), pp.22. ⟨10.1038/s41431-023-01367-z⟩. ⟨hal-04092022⟩
- L. Benarroch, I. Nelson, T. Stojkovic, B Mohand Oumoussa, H. Madry, et al.. P166 Deciphering the genetic cause of oculopharyngodistal myopathy in a French cohort using Cas9-targeted long-read sequencing. 28th International Annual Congress of the World Muscle Society, Oct 2023, Charleston SC, United States. pp.S141, ⟨10.1016/j.nmd.2023.07.298⟩. ⟨hal-04280249⟩
- Amira Bouzidi, Karim Labreche, Marine Baron, Marianne Veyri, Jérôme Alexandre Denis, et al.. Low-Coverage Whole Genome Sequencing of Cell-Free DNA From Immunosuppressed Cancer Patients Enables Tumor Fraction Determination and Reveals Relevant Copy Number Alterations. Frontiers in Cell and Developmental Biology, 2021, 9, pp.661272. ⟨10.3389/fcell.2021.661272⟩. ⟨hal-03363081⟩
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