F Devillard
Overview
Explore the profile of F Devillard including associated specialties, affiliations and a list of published articles.
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Articles
15
Citations
138
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Recent Articles
1.
Smol T, Petit F, Piton A, Keren B, Sanlaville D, Afenjar A, et al.
Neurogenetics
. 2018 Mar;
19(2):93-103.
PMID: 29511999
Molecular anomalies in MED13L, leading to haploinsufficiency, have been reported in patients with moderate to severe intellectual disability (ID) and distinct facial features, with or without congenital heart defects. Phenotype...
2.
El Chehadeh S, Touraine R, Prieur F, Reardon W, Bienvenu T, Chantot-Bastaraud S, et al.
Clin Genet
. 2016 Oct;
91(4):576-588.
PMID: 27761913
Duplication of the Xq28 region, involving MECP2 (dupMECP2), has been primarily described in males with severe developmental delay, spasticity, epilepsy, stereotyped movements and recurrent infections. Carrier mothers are usually asymptomatic...
3.
Pilorge M, Fassier C, Le Corronc H, Potey A, Bai J, De Gois S, et al.
Mol Psychiatry
. 2015 Sep;
21(7):936-45.
PMID: 26370147
Autism spectrum disorder (ASD) is a common neurodevelopmental condition characterized by marked genetic heterogeneity. Recent studies of rare structural and sequence variants have identified hundreds of loci involved in ASD,...
4.
David M, Billette de Villemeur A, Devillard F, Dieterich K, Jouk P, Prado C, et al.
Arch Pediatr
. 2015 Feb;
22(3):223-34.
PMID: 25656456
Studies on mild intellectual disability (MID) are scarce. The aim of this study was to describe the educational and medical care trajectories and their determinants in children with MID. The...
5.
Coutton C, Poreau B, Devillard F, Durand C, Odent S, Rozel C, et al.
Mol Syndromol
. 2014 Feb;
5(1):25-31.
PMID: 24550762
Holoprosencephaly (HPE) is the most common forebrain defect in humans. It results from incomplete midline cleavage of the prosencephalon and can be caused by environmental and genetic factors. HPE is...
6.
Coutton C, Bidart M, Rendu J, Devillard F, Vieville G, Amblard F, et al.
Clin Genet
. 2013 Mar;
84(6):596-9.
PMID: 23521658
No abstract available.
7.
Faure A, Aknin-Seifer I, Satre V, Amblard F, Devillard F, Hennebicq S, et al.
Hum Reprod
. 2007 Jun;
22(7):1854-60.
PMID: 17582144
Background: Cytogenetically detectable aberrations of the Y chromosome, such as isodicentrics, rings or translocations are sometimes associated with male non-obstructive infertility. This report presents a detailed analysis of the clinical,...
8.
Faure A, Devillard F, Sele B, Hennebicq S
J Gynecol Obstet Biol Reprod (Paris)
. 2005 Jun;
34(1 Pt 2):1S39-43.
PMID: 15968787
No abstract available.
9.
Satre V, Monnier N, Devillard F, Amblard F, Lunardi J
Prenat Diagn
. 2004 Nov;
24(11):913-7.
PMID: 15565644
Objectives: We report on a prenatal diagnosis of DMD complicated by a 45,X karyotype that was revealed only in the chorionic villus long-term culture. Methods: Cytogenetic investigations were performed on...
10.
Luquet I, Mugneret F, Athis P, Nadal N, Favre B, Abel C, et al.
Ann Genet
. 2002 Jul;
45(2):77-88.
PMID: 12119216
This prospective and multi-centric study confirms the accuracy and the limitations of interphase FISH and shows that any cytogenetics laboratory can perform this technique. With regard to the technical approach,...