Solveig Heide - Dissemin

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All papers authored by Solveig Heide

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2021 Anushree Acharya, Haluk Kavus, Patrick Dunn, Abdul Nasir, Leandra Folk, Kara Withrow, Ingrid M. Wentzensen, Maura R. Z. Ruzhnikov, Camille Fallot, Thomas Smol, Mélanie Rama, Kathleen Brown, Sandra Whalen, Alban Ziegler, Magali Barth and 21 other authors

Delineating the genotypic and phenotypic spectrum of HECW2-related neurodevelopmental disorders

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2020 Solveig Heide

ORCID

, Myrtille Spentchian, Stéphanie Valence, Julien Buratti, Corinne Mach, Elodie Lejeune, Valérie Olin, Marta Massimello, Daphné Lehalle, Linda Mouthon, Sandra Whalen, Anne Faudet, Cyril Mignot, Catherine Garel, Eleonore Blondiaux and 31 other authors

Prenatal exome sequencing in 65 fetuses with abnormality of the corpus callosum: contribution to further diagnostic delineation

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2019 Karin Weiss

ORCID

, Hayley P. Lazar

ORCID

, Alina Kurolap

ORCID

, Ariel F. Martinez

ORCID

, Tamar Paperna, Lior Cohen

ORCID

, Marie F. Smeland, Sandra Whalen, Solveig Heide

ORCID

ORCID

, Pauline Terhal, Melita Irving, Motoki Takaku

ORCID

, John D. Roberts, Robert M. Petrovich and 34 other authors

The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis

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This paper was not found in any repository, but could be made available legally by the author.

2017 Solveig Heide

ORCID

, Boris Keren, Thierry Billette de Villemeur, Sandra Chantot-Bastaraud, Christel Depienne, Caroline Nava, Cyril Mignot, Aurélia Jacquette, Eric Fonteneau, Elodie Lejeune, Corinne Mach, Isabelle Marey, Sandra Whalen, Didier Lacombe

ORCID

, Sophie Naudion and 15 other authors

Copy Number Variations Found in Patients with a Corpus Callosum Abnormality and Intellectual Disability

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This paper was not found in any repository, but could be made available legally by the author.

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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