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Статьи в журналах
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- 2016 Functional characterization of a human POU1F1 mutation associated with isolated growth hormone deficiency: a novel etiology for IGHD
- Sobrier ML, Perez C., Leheup B., Bouceba T., Duquesnoy P., Chopin B., Sizova D., Penza A.
- в журнале Human Molecular Genetics, издательство Oxford University Press (United Kingdom), том 25, № 3, с. 472-483