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|Sobrier ML, Tsai YC, Pérez C, et al. (2015) Functional characterization of a human POU1F1 mutation associated with isolated growth hormone deficiency (IGHD): a novel etiology for IGHD. Human Molecular Genetics|
|Sobrier ML, Brachet C, ViÃ©-Luton MP, et al. (2012) Symptomatic heterozygotes and prenatal diagnoses in a nonconsanguineous family with syndromic combined pituitary hormone deficiency resulting from two novel LHX3 mutations. The Journal of Clinical Endocrinology and Metabolism. 97: E503-9|
|Malinge S, Ragu C, Della-Valle V, et al. (2008) Activating mutations in human acute megakaryoblastic leukemia. Blood. 112: 4220-6|