Publications by authors named "Fanny Ferroul"

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Rare features in Feingold syndrome type 1.
Fanny Ferroul, Sarah Snanoudj, Gaëlle Leterme, Kheira Mezouaghi, Marie Kieffer-Traversier

Eur J Med Genet· December 2025

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First Description of a Large Clinical Series of Fetal Alcohol Spectrum Disorders Children and Adolescents in Reunion Island, France.
Laëtitia Sennsfelder, Susie Guilly, Sonia Henkous, Christophe Lebon, Sébastien Leruste, Fanny Ferroul

Children (Basel)· August 2024

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Prenatal and neonatal phenotype of Larsen of La Réunion Island syndrome (B4GALT7-linkeropathy).
Jean-Luc Alessandri, Tristan Celse, Marta Spodenkiewicz, Anais Calaya, Coralie Dumont, Fanny Ferroul

Eur J Med Genet· June 2024

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Lessons from two series by physicians and caregivers' self-reported data in DDX3X-related disorders.
Valentin Ruault, Pauline Burger, Johanna Gradels-Hauguel, Nathalie Ruiz, , Fanny Ferroul

Mol Genet Genomic Med· January 2024

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STAC3 related congenital myopathy: A case series of seven Comorian patients.
Marie Gromand, Paul Gueguen, Anne Pervillé, Fanny Ferroul, Godelieve Morel

Eur J Med Genet· October 2022

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