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Poster De Conférence Année : 2019

Novel OTX2 gene mutations causing combined pituitary hormone deficiency without ocular anomalies.

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inserm-04164968 , version 1 (18-07-2023)

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  • HAL Id : inserm-04164968 , version 1

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Oliver Heath, Melissa C. Edwards, Himanshu Goel, Marie Legendre, Serge Amselem, et al.. Novel OTX2 gene mutations causing combined pituitary hormone deficiency without ocular anomalies.. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Sep 2019, Adelaide, SA, Australia. ⟨inserm-04164968⟩
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