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Article

Isolated growth hormone deficiency due to the R183H mutation in GH1: Clinical analysis of a four-generation family.

Clinical endocrinology - 1 Dec 2017

Cabrera-Salcedo Catalina, Shah Amy S, Andrew Melissa, Tyzinski Leah, Hwa Vivian, Gutmark-Little Iris, Backeljauw Philippe, Dauber Andrew

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PMID: 28626954
DOI: 10.1111/cen.13400
PMCID: PMC5698139

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