Alinoe Lavillaureix - Dissemin

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All papers authored by Alinoe Lavillaureix

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2023 Thomas Husson

ORCID

, François Lecoquierre, Gaël Nicolas

ORCID

, Anne-Claire Richard, Alexandra Afenjar, Séverine Audebert-Bellanger, Catherine Badens, Frédéric Bilan, Varoona Bizaoui, Anne Boland, Marie-Noëlle Bonnet-Dupeyron, Elise Brischoux-Boucher

ORCID

, Céline Bonnet

ORCID

, Marie Bournez

ORCID

, Odile Boute and 89 other authors

Episignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders

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2021 Auriane Cospain

ORCID

, Lionel Van Maldergem, Elise Schaefer, Marie Faoucher, Christèle Dubourg, Wilfrid Carré, Varoona Bizaoui, Jessica Assoumani, Amélie Piton, Bénédicte Gérard, Ange‐Line Bruel

ORCID

, Laurence Faivre, Florence Demurger, Laurent Pasquier

ORCID

, Sylvie Odent and 3 other authors

Skraban-Deardorff syndrome: Six new cases of WDR26-related disease and expansion of the clinical phenotype.

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2019 Anne H. O’Donnell-Luria, Lynn S. Pais, Víctor Faundes, Jordan C. Wood, Abigail Sveden, Victor Luria, Rami Abou Jamra, Andrea Accogli, Kimberly Amburgey, Britt Marie Anderlid, Silvia Azzarello-Burri, Alice A. Basinger, Claudia Bianchini, Lynne M. Bird, Rebecca Buchert and 369 other authors

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

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2017 E. Chérot, B. Keren, C. Dubourg, W. Carré, M. Fradin, A. Lavillaureix

ORCID

, A. Afenjar, L. Burglen, S. Whalen, P. Charles, I. Marey, S. Heide, A. Jacquette, D. Heron, D. Doummar and 15 other authors

Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients

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A. Lavillaureix

ORCID

, S. Heide, S. Chantot-Bastaraud, I. Marey, B. Keren, R. Grigorescu, J. M. Jouannic, A. Gelot, S. Whalen, D. Héron, J. P. Siffroi

Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly

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Ileena Mitra

ORCID

, Alinoë Lavillaureix

ORCID

ORCID

, Michela Traglia, Kathryn Tsang, Carrie E. Bearden

ORCID

, Katherine A. Rauen, Lauren A. Weiss

ORCID

Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders

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2015 Solveig Heide

ORCID

, Jean-Pierre Siffroi, Alexandra Afenjar, Patrick Edery, Damien Sanlaville, Boris Keren, Alexandre Rouen, Alinoë Lavillaureix

ORCID

, Capucine Hyon, Diane Doummar, Siffroi Jp, Sandra Chantot-Bastaraud

Xp21 deletion in female patients with intellectual disability: Two new cases and a review of the literature

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Alexandre Rouen, Alinoë Lavillaureix

ORCID

, Jean-Pierre Siffroi, Capucine Hyon, Solveig Heide, Sylvain Clède, Richard Balet, Esther Kott

ORCID

, Nino Guy Cassuto

ORCID

, Cassuto Ng, Siffroi Jp

Nuclear volume differences between balanced and unbalanced spermatozoa in chromosomal translocation carriers

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