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Article

Association of the exon 3 deleted/full-length GHR polymorphism with recombinant growth hormone dose in growth hormone-deficient adults.

Pharmacogenomics - 1 Oct 2009

Meyer Silke, Schaefer Stephan, Stolk Lisette, Arp Pascal, Uitterlinden André G, Plöckinger Ursula, Stalla Günter K, Tuschy Ulrich, Weber Matthias M, Weise Alexander, Pfützner Andreas, Kann Peter H

Abstract excerpt

AIMS: Contradictory reports exist regarding the influence of the exon 3 deleted (d3)/full-length (fl) growth hormone receptor (GHR) polymorphism on responsiveness to recombinant human growth-hormone therapy in idiopathic short stature, small for gestational age and GH-deficient children, Turner syndrome patients and GH-deficient adults. In some of these studies, the d3 allele was associated with increased...

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Source

Identifiers

PMID: 19842933
DOI: 10.2217/pgs.09.91

Genes

GHR
SDS

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Association of the exon 3 deleted/full-length GHR polymorphism with recombinant growth hormone dose in growth hormone-deficient adults.PMID 19842933Read ↗

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