Failure of digit tip regeneration in the absence of Lmx1b suggests Lmx1b functions disparate from dorsoventral polarity
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Published in Cell reports (Cambridge) (31.01.2023)
Published in Cell reports (Cambridge) (31.01.2023)
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Published in Pathology (01.08.2011)
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14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements
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Published in European journal of human genetics : EJHG (27.06.2012)
Published in European journal of human genetics : EJHG (27.06.2012)
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Published in Nature (London) (01.04.2021)
Published in Nature (London) (01.04.2021)
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Noncoding copy-number variations are associated with congenital limb malformation
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Published in Genetics in medicine (01.06.2018)
Published in Genetics in medicine (01.06.2018)
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WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlation
Mignot, Cyril, Lambert, Laetitia, Pasquier, Laurent, Bienvenu, Thierry, Delahaye-Duriez, Andrée, Keren, Boris, Lefranc, Jérémie, Saunier, Aline, Allou, Lila, Roth, Virginie, Valduga, Mylène, Moustaïne, Aissa, Auvin, Stéphane, Barrey, Catherine, Chantot-Bastaraud, Sandra, Lebrun, Nicolas, Moutard, Marie-Laure, Nougues, Marie-Christine, Vermersch, Anne-Isabelle, Héron, Bénédicte, Pipiras, Eva, Héron, Delphine, Olivier-Faivre, Laurence, Guéant, Jean-Louis, Jonveaux, Philippe, Philippe, Christophe
Published in Journal of medical genetics (01.01.2015)
Published in Journal of medical genetics (01.01.2015)
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14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements
Allou, Lila, Lambert, Laetitia, Amsallem, Daniel, Bieth, Eric, Edery, Patrick, Destrée, Anne, Rivier, François, Amor, David, Thompson, Elizabeth, Nicholl, Julian, Harbord, Michael, Nemos, Christophe, Saunier, Aline, Moustaïne, Aissa, Vigouroux, Adeline, Jonveaux, Philippe, Philippe, Christophe
Published in European journal of human genetics : EJHG (01.12.2012)
Published in European journal of human genetics : EJHG (01.12.2012)
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RUNX1T1, a chromatin repression protein, is a candidate gene for autosomal dominant intellectual disability
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Published in American journal of medical genetics. Part A (01.07.2012)
Published in American journal of medical genetics. Part A (01.07.2012)
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RUNXIT1, a chromatin repression protein, is a candidate gene for autosomal dominant intellectual disability
TUAN HUYNH, Minh, BERI-DEXHEIMER, Mylène, BONNET, Céline, BRONNER, Myriam, ALI KHAN, Asma, ALLOU, Lila, PHILIPPE, Christophe, VIGNERON, Jacqueline, JONVEAUX, Philippe
Published in American journal of medical genetics. Part A (2012)
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Published in American journal of medical genetics. Part A (2012)
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An adult patient with 49, XXXXY syndrome: further clinical and biological delineation
Collet, Agnès, Chatelin, Jérôme, Agopiantz, Mikaël, Valduga, Mylène, Bonnet, Céline, Allou, Lila, Lambert, Laëtitia, Gospodaru, Razvan Nicolaie, Weryha, Georges, Jonveaux, Philippe
Published in Annales de biologie clinique (Paris) (01.05.2014)
Published in Annales de biologie clinique (Paris) (01.05.2014)
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Journal Article
Failure of digit tip regeneration in the absence of suggests Lmx1b functions disparate from dorsoventral polarity
Castilla-Ibeas, Alejandro, Zdral, Sofia, Galan, Laura, Haro, Endika, Allou, Lila, Campa, Victor M, Icardo, Jose M, Mundlos, Stefan, Oberg, Kerby C, Ros, Marian
Published in bioRxiv (05.05.2022)
Published in bioRxiv (05.05.2022)
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