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5. Phenotypic spectrum and responses to recombinant human IGF1 (rhIGF1) therapy in patients with homozygous intronic pseudoexon growth hormone receptor mutation. Issue 5 (May 2018)

7. Rare CNVs provide novel insights into the molecular basis of GH and IGF-1 insensitivity. Issue 6 (December 2020)

8. Rare CNVs provide novel insights into the molecular basis of GH and IGF-1 insensitivity. Issue 6 (December 2020)