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First evidence of SOX2 mutations in Peters' anomaly: Lesson..:
Chesneau, Bertrand
;
Aubert-Mucca, Marion
;
Fremont, Felix
...
info:eu-repo/semantics/altIdentifier/doi/10.1111/cge.14123. , 2022
Link:
https://hal.science/hal-03610074
RT Journal T1
First evidence of SOX2 mutations in Peters' anomaly: Lessons from molecular screening of 95 patients
UL https://suche.suub.uni-bremen.de/peid=base-ftunivparis:oai:HAL:hal-03610074v1&Exemplar=1&LAN=DE A1 Chesneau, Bertrand A1 Aubert-Mucca, Marion A1 Fremont, Felix A1 Pechmeja, Jacmine A1 Soler, Vincent A1 Isidor, Bertrand A1 Nizon, Mathilde A1 Dollfus, Helene A1 Kaplan, Josseline A1 Fares-Taie, Lucas A1 Rozet, Jean-Michel A1 Busa, Tiffany A1 Lacombe, Didier A1 Naudion, Sophie A1 Amiel, Jeanne A1 Rio, Marlene A1 Attie-Bitach, Tania A1 Lesage, Cecile A1 Thouvenin, Dominique A1 Odent, Sylvie A1 Morel, Godelieve A1 Vincent-Delorme, Catherine A1 Boute, Odile A1 Vanlerberghe, Clemence A1 Dieux, Anne A1 Boussion, Simon A1 Faivre, Laurence A1 Pinson, Lucile A1 Laffargue, Fanny A1 Le Guyader, Gwenael A1 Le Meur, Guylène A1 Prieur, Fabienne A1 Lambert, Victor A1 Laudier, Beatrice A1 Cottereau, Edouard A1 Ayuso, Carmen A1 Corton-Perez, Marta A1 Bouneau, Laurence A1 Le Caignec, Cedric A1 Gaston, Veronique A1 Jeanton-Scaramouche, Claire A1 Dupin-Deguine, Delphine A1 Calvas, Patrick A1 Chassaing, Nicolas A1 Plaisancie, Julie PB HAL CCSD; Wiley YR 2022 K1 anterior segment dysgenesis K1 B3GLCT K1 CNV K1 FOXE3 K1 microphthalmia K1 PAX6 K1 Peters' anomaly K1 PITX3 K1 SOX2 K1 [SDV]Life Sciences [q-bio] K1 [SDV.GEN]Life Sciences [q-bio]/Genetics JF info:eu-repo/semantics/altIdentifier/doi/10.1111/cge.14123 LK http://dx.doi.org/https://hal.science/hal-03610074 DO https://hal.science/hal-03610074 SF ELIB - SuUB Bremen
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