Marie-Pierre Alex-Cordier
Overview
Explore the profile of Marie-Pierre Alex-Cordier including associated specialties, affiliations and a list of published articles.
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Articles
2
Citations
38
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Recent Articles
1.
Blepharocheilodontic syndrome is a CDH1 pathway-related disorder due to mutations in CDH1 and CTNND1
Ghoumid J, Stichelbout M, Jourdain A, Frenois F, Lejeune-Dumoulin S, Alex-Cordier M, et al.
Genet Med
. 2017 Mar;
19(9):1013-1021.
PMID: 28301459
Purpose: Blepharocheilodontic (BCD) syndrome is a rare autosomal dominant condition characterized by eyelid malformations, cleft lip/palate, and ectodermal dysplasia. The molecular basis of BCD syndrome remains unknown. Methods: We recruited...
2.
Jedraszak G, Demeer B, Mathieu-Dramard M, Andrieux J, Receveur A, Weber A, et al.
Am J Med Genet A
. 2015 Jan;
167A(3):504-11.
PMID: 25572454
Interstitial microdeletions of 20q chromosome are rare, only 17 patients have been reported in the literature to date. Among them, only six carried a proximal 20q11.21-q11.23 deletion, with a size...