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Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|June 29, 2023
Disruption of regulatory domains and novel transcripts as disease-causing mechanismsLila Allou, Stefan MundlosAnnales De Biologie Clinique|May 31, 2014
[An adult patient with 49, XXXXY syndrome: further clinical and biological delineation]Agnès Collet, Jérôme Chatelin, Mikaël Agopiantz, et al.Pathology|July 1, 2011
BRAF, p53 and SOX2 in anaplastic thyroid carcinoma: evidence for multistep carcinogenesisGuillaume Gauchotte, Christophe Philippe, Stéphanie Lacomme, et al.Cell Reports|January 15, 2023
Failure of digit tip regeneration in the absence of Lmx1b suggests Lmx1b functions disparate from dorsoventral polarityAlejandro Castilla-Ibeas, Sofía Zdral, Laura Galán, et al.Genes & Development|April 15, 2026
Temporal loss of <i>En1</i> during limb development causes distinct phenotypesAlessa R Ringel, Natalia Benetti, Andreas Magg, et al.European Journal of Human Genetics : EJHG|June 29, 2012
14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elementsLila Allou, Laetitia Lambert, Daniel Amsallem, et al.Journal of Medical Genetics|November 21, 2014
WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlationCyril Mignot, Laetitia Lambert, Laurent Pasquier, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 14, 2017
Noncoding copy-number variations are associated with congenital limb malformationRicarda Flöttmann, Bjørt K Kragesteen, Sinje Geuer, et al.Nature|February 11, 2021
Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulatorLila Allou, Sara Balzano, Andreas Magg, et al.Pageof 1