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  1. Jaureguiberry, Graciana [Author]; De la Dure-Molla, Muriel [Author]; Parry, David [Author]; Quentric, Mickael [Author]; Himmerkus, Nina [Author]; Koike, Toshiyasu [Author]; Poulter, James [Author]; Klootwijk, Enriko [Author]; Robinette, Steven L. [Author]; Howie, Alexander J. [Author]; Patel, Vaksha [Author]; Figueres, Marie-Lucile [Author]; Stanescu, Horia C. [Author]; Issler, Naomi [Author]; Nicholson, Jeremy K. [Author]; Bockenhauer, Detlef [Author]; Laing, Christopher [Author]; Walsh, Stephen B. [Author]; McCredie, David A. [Author]; Povey, Sue [Author]; Asselin, Audrey [Author]; Picard, Arnaud [Author]; Coulomb, Aurore [Author]; Medlar, Alan J. [Author]; [...]

    Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutationsNephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal RecessiveFAM20AMutations

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    Basel: Karger, 23 February 2013

    Published in: Nephron. Physiology ; 122 (2012), 1-2

  13. Thomas, Charlotte; Vaysse, Frédéric; Courset, Teva; Nasr, Karim; Courtois, Bruno; L’Homme, Arnaud; Chassaing, Nicolas; Vinel, Alexia; Bailleul-Forestier, Isabelle; Raynaldy, Luc; Laurencin-Dalicieux, Sara

    From Child to Adulthood, a Multidisciplinary Approach of Multiple Microdontia Associated with Hypodontia: Case Report Relating a 15 Year-Long Management and Follow-Up

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    MDPI AG, 2021

    Published in: Healthcare

  14. Esclassan, Rémi; Valera, Marie-Cécile; Bergia, Jean Marc; Canceill, Thibault; Mendes, Leonor Costa; Bailleul-Forestier, Isabelle; Gardette, Virginie; Vaysse, Frédéric; Gurgel-Georgelin, Marie; Noirrit, Emmanuelle

    Morbidity and Mortality Review in a University Dental Hospital: A Necessary Tool to Improve Quality of Care

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    Georg Thieme Verlag KG, 2021

    Published in: European Journal of Dentistry

  15. Lévy, Jonathan; Capri, Yline; Rachid, Myriam; Dupont, Céline; Vermeesch, Joris R.; Devriendt, Koen; Verloes, Alain; Tabet, Anne‐Claude; Bailleul‐Forestier, Isabelle

    LEF1 haploinsufficiency causes ectodermal dysplasia

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    Wiley, 2020

    Published in: Clinical Genetics

  16. Poelmans, Simon; Kawamoto, Tatsuro; Cristofoli, Francesca; Politis, Constantinus; Vermeesch, Joris; Bailleul‐Forestier, Isabelle; Hens, Greet; Devriendt, Koenraad; Verdonck, Anna; Carels, Carine

    Genotypic and phenotypic variation in six patients with solitary median maxillary central incisor syndrome

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    Wiley, 2015

    Published in: American Journal of Medical Genetics Part A

  17. Rifai, Laila; Port‐Lis, Marylin; Tabet, Anne‐Claude; Bailleul‐Forestier, Isabelle; Benzacken, Brigitte; Drunat, Séverine; Kuzbari, Suzanne; Passemard, Sandrine; Verloes, Alain; Aboura, Azzedine

    Ectodermal dysplasia‐like syndrome with mental retardation due to contiguous gene deletion: Further clinical and molecular delineation of del(2q32) syndrome

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    Wiley, 2010

    Published in: American Journal of Medical Genetics Part A

  18. Guilmin-Crépon, Sophie; Garel, Catherine; Baumann, Clarisse; Brémond-Gignac, Dominique; Bailleul-Forestier, Isabelle; Magnier, Suzel; Castanet, Mireille; Czernichow, Paul; Van Den Abbeele, Thierry; Léger, Juliane

    High Proportion of Pituitary Abnormalities and Other Congenital Defects in Children with Congenital Nasal Pyriform Aperture Stenosis

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    Springer Science and Business Media LLC, 2006

    Published in: Pediatric Research

  19. Gasse, Barbara; Prasad, Megana; Delgado, Sidney; Huckert, Mathilde; Kawczynski, Marzena; Garret-Bernardin, Annelyse; Lopez-Cazaux, Serena; Bailleul-Forestier, Isabelle; Manière, Marie-Cécile; Stoetzel, Corinne; Bloch-Zupan, Agnès; Sire, Jean-Yves

    Evolutionary Analysis Predicts Sensitive Positions of MMP20 and Validates Newly- and Previously-Identified MMP20 Mutations Causing Amelogenesis Imperfecta

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    Frontiers Media SA, 2017

    Published in: Frontiers in Physiology

  20. Plaisancié, Julie; Bailleul‐Forestier, Isabelle; Gaston, Véronique; Vaysse, Fréderic; Lacombe, Didier; Holder‐Espinasse, Muriel; Abramowicz, Marc; Coubes, Christine; Plessis, Ghislaine; Faivre, Laurence; Demeer, Bénédicte; Vincent‐Delorme, Catherine; Dollfus, Hélène; Sigaudy, Sabine; Guillén‐Navarro, Encarna; Verloes, Alain; Jonveaux, Philippe; Martin‐Coignard, Dominique; Colin, Estelle; Bieth, Eric; Calvas, Patrick; Chassaing, Nicolas

    Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia

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    Wiley, 2013

    Published in: American Journal of Medical Genetics Part A