Condition: Short Stature, Idiopathic, Autosomal


rs121909361 in GHR gene and Short Stature, Idiopathic, Autosomal PMID 7565946 1995 Mutations of the growth hormone receptor in children with idiopathic short stature. The Growth Hormone Insensitivity Study Group.

rs121917883 in GHSR gene and Short Stature, Idiopathic, Autosomal PMID 16511605 2006 Loss of constitutive activity of the growth hormone secretagogue receptor in familial short stature.

PMID 19789204 2009 Recessive isolated growth hormone deficiency and mutations in the ghrelin receptor.