Jeanne Jury
3PUBLICATIONS
5CO-AUTHORS
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Publications (3)
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|Sep 17, 2025
Heterozygous alterations of GTF2I at the Williams-Beuren syndrome's locus cause a neurodevelopmental disorder.Jeanne Jury, Thomas Besnard, Wallid Deb
|Aug 08, 2024
Prenatal Diagnosis of Myhre Syndrome in Two Cases: Further Delineation of the Cardiac and External Phenotype.Jeanne Jury, Madeleine Joubert, Claudine Le Vaillant
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