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Elsevier, European Journal of Medical Genetics, 4(63), p. 103773, 2020

DOI: 10.1016/j.ejmg.2019.103773

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Patients with 10q22.3q23.1 recurrent deletion syndrome are at risk for juvenile polyposis

Journal article published in 2019 by François Lecoquierre ORCID, Kévin Cassinari, Pascal Chambon, Gaël Nicolas, Sarah Malsa, Régine Marlin, Yvon Assouline, J. F. Fl?jou, Jean-François Fléjou, Thierry Frebourg, Claude Houdayer, Odile Bera, Stéphanie Baert-Desurmont
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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