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Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency |
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| Authors: | Netchine I Sobrier M L Krude H Schnabel D Maghnie M Marcos E Duriez B Cacheux V Moers A v Goossens M Grüters A Amselem S |
| Institution: | [1] Laboratoire de Génétique et de Physiopathologie, Institut National de la Santé et de la Recherche Médicale (INSERM) U.468, H?pital Henri-Mondor, Créteil, France. |
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| 本文献已被 PubMed 等数据库收录！ | |