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Brain : a Journal of Neurology|September 4, 2025
A large cohort study of prenatal exome sequencing redefines diagnosis in fetal corpus callosum anomaliesDelphine Héron, Anna Gerasimenko, Lisa Frugère, et al.
Gynecologie, Obstetrique, Fertilite & Senologie|January 30, 2025
[Management of women with abnormal cervical cytology: Update of INCa recommendations after the implementation of HPV screening]Jean-Luc Brun, Christine Bergeron, Gerlinde Averous, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|September 16, 2025
Management of women with abnormal cervical cytology: Update of French guidelines after the implementation of HPV screeningJ L Brun, C Bergeron, G Averous, et al.
Genes|September 28, 2023
Snijders Blok-Campeau Syndrome: Description of 20 Additional Individuals with Variants in <i>CHD3</i> and Literature ReviewPatricia Pascual, Jair Tenorio-Castano, Cyril Mignot, et al.
Clinical Genetics|January 8, 2021
Clinical and neuroimaging findings in 33 patients with MCAP syndrome: A survey to evaluate relevant endpoints for future clinical trialsAurore Garde, Laurent Guibaud, Alice Goldenberg, et al.
Brain : a Journal of Neurology|May 21, 2013
β-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulationSusan J Hayflick, Michael C Kruer, Allison Gregory, et al.
Gynecologie, Obstetrique, Fertilite & Senologie|May 31, 2023
[Pelvic exam in gynecology and obstetrics: Guidelines for clinical practice]Xavier Deffieux, Christine Rousset-Jablonski, Adrien Gantois, et al.
Rhinology|July 14, 2025
Olfactory implants: international opinion paper on emerging technologies and clinical applicationsK L Whitcroft, A K Hernandez, P Andrews, et al.
Nature Communications|November 3, 2022
Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome XElsa Leitão, Christopher Schröder, Ilaria Parenti, et al.
Journal of Medical Genetics|June 29, 2021
Recurrent <i>de novo</i> missense variants in <i>GNB2</i> can cause syndromic intellectual disabilityNatalie B Tan, Alistair T Pagnamenta, Matteo P Ferla, et al.
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