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Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency von Moers, Arpard v, Marcos, Elisabeth, Goossens, Michel, Schnabel, Dirk, Netchine, Irène, Maghnie, Mohamed, Amselem, Serge, Duriez, Bénédicte, Grüters, Annette, Sobrier, Marie-Laure, Krude, Heiko, Cacheux, Valère
Veröffentlicht in Nature genetics
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