Severe growth failure associated with a novel heterozygous nonsense mutation in the GHR transmembrane domain leading to elevated growth hormone binding protein

Growth Hormone Receptor Mutations Related to Individual Dwarfism

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Fifty seven years of follow-up of the Israeli cohort of Laron Syndrome patients—From discovery to treatment

(2016) Zvi Laron et al.   GROWTH HORMONE & IGF RESEARCH

Growth hormone binding protein – Physiological and analytical aspects

(2015) Katharina Schilbach et al.   BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM

Clinical and biochemical consequences of an intragenic growth hormone receptor (GHR) deletion in a large Chinese pedigree

(2014) Jürgen Klammt et al.   CLINICAL ENDOCRINOLOGY

The Insulin-Like Growth Factors and Growth Disorders of Childhood

(2012) Philippe F. Backeljauw et al.   ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA

The Growth Hormone Receptor (GHR)c.899dupCMutation Functions as a Dominant Negative: Insights into the Pathophysiology of IntracellularGHRDefects

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Atypical GH Insensitivity Syndrome and Severe Insulin-Like Growth Factor-I Deficiency Resulting from Compound Heterozygous Mutations of the GH Receptor, Including a Novel Frameshift Mutation Affecting the Intracellular Domain

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