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Complex disease phenotype revealed by GH deficiency associated with a novel and unusual defect in the GH-1 gene
Authors:Iughetti Lorenzo  Sobrier Marie-Laure  Predieri Barbara  Netchine Irene  Carani Cesare  Bernasconi Sergio  Balli Fiorella  Amselem Serge
Affiliation:Departments of Paediatrics and;Endocrinology, Universities of Modena and Reggio Emilia, and Parma, Italy and;INSERM U654, Hôpital Armand-Trousseau, Paris 75012, France
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