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GGCX-related congenital combined vitamin K-dependent clotting factors deficiency-1: Description of a fetus with chondrodysplasia punctata.
Am J Med Genet A. 2022 Jan;188(1):314-318. doi: 10.1002/ajmg.a.62503. Epub 2021 Sep 24.
Am J Med Genet A. 2022.
PMID: 34558179
Genetic mutation risk calculation in Lynch syndrome inheritance: Evaluating the utility of the PREMM1,2,6 model in Lyon: The first French study.
Aissaoui S, Cartellier C, Seytier T, Giraud S, Calender A.
Aissaoui S, et al. Among authors: cartellier c.
Bull Cancer. 2017 Mar;104(3):288-294. doi: 10.1016/j.bulcan.2016.11.017. Epub 2016 Dec 27.
Bull Cancer. 2017.
PMID: 28038733
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