Variability of isolated autosomal dominant GH deficiency (IGHD II): impact of the P89L GH mutation on clinical follow-up and GH secretion.
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I. Robinson | P. Czernichow | G. Binder | S. Yousefi | P. Mullis | K. Baltensperger | E. Sonnet | S. Salemi | D. Simon | A. Eblé