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Patients with 10q22.3q23.1 recurrent deletion syndrome are ..:
Lecoquierre, François
;
Cassinari, Kévin
;
Chambon, Pascal
...
European Journal of Medical Genetics. 63 (2020) 4 - p. 103773 , 2020
Link:
https://doi.org/10.1016/j.ejmg.2019.103773
RT Journal T1
Patients with 10q22.3q23.1 recurrent deletion syndrome are at risk for juvenile polyposis
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ejmg.2019.103773&Exemplar=1&LAN=DE A1 Lecoquierre, François A1 Cassinari, Kévin A1 Chambon, Pascal A1 Nicolas, Gaël A1 Malsa, Sarah A1 Marlin, Régine A1 Assouline, Yvon A1 Fléjou, Jean-François A1 Frebourg, Thierry A1 Houdayer, Claude A1 Bera, Odile A1 Baert-Desurmont, Stéphanie PB Elsevier BV YR 2020 SN 1769-7212 JF European Journal of Medical Genetics VO 63 IS 4 SP 103773 LK http://dx.doi.org/https://doi.org/10.1016/j.ejmg.2019.103773 DO https://doi.org/10.1016/j.ejmg.2019.103773 SF ELIB - SuUB Bremen
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