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Complex disease phenotype revealed by GH deficiency associated with a novel and unusual defect in the GH-1 gene

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Document Type: Research Article

Affiliations: 1: Departments of Paediatrics and 2: INSERM U654, Hôpital Armand-Trousseau, Paris 75012, France, Email: [email protected] 3: Endocrinology, Universities of Modena and Reggio Emilia, and Parma, Italy and

Publication date: July 1, 2008

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