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Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.
Am J Hum Genet. 2021 Oct 7;108(10):1907-1923. doi: 10.1016/j.ajhg.2021.09.003. Epub 2021 Sep 30.
Am J Hum Genet. 2021.
PMID: 34597585
Free PMC article.
Patients with 10q22.3q23.1 recurrent deletion syndrome are at risk for juvenile polyposis.
Lecoquierre F, Cassinari K, Chambon P, Nicolas G, Malsa S, Marlin R, Assouline Y, Fléjou JF, Frebourg T, Houdayer C, Bera O, Baert-Desurmont S.
Lecoquierre F, et al. Among authors: malsa s.
Eur J Med Genet. 2020 Apr;63(4):103773. doi: 10.1016/j.ejmg.2019.103773. Epub 2019 Sep 24.
Eur J Med Genet. 2020.
PMID: 31561016
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Mutation HOXB13 c.853delT in Martinican prostate cancer patients.
Marlin R, Créoff M, Merle S, Jean-Marie-Flore M, Rose M, Malsa S, Promeyrat X, Martin F, Comlan G, Rabia N, Taouil T, Issoufaly I, Escarmant P, Vinh-Hung V, Béra O.
Marlin R, et al. Among authors: malsa s.
Prostate. 2020 May;80(6):463-470. doi: 10.1002/pros.23960. Epub 2020 Feb 10.
Prostate. 2020.
PMID: 32040869
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