Mutations in GH1 gene and isolated growth hormone deficiency (IGHD): A familial case of IGHD type I and systematic review
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference32 articles.
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3. Growth hormone antibodies in patients treated with different preparations of human growth hormone (HGH);Illig;J. Clin. Endocrinol. Metab.,1970
4. Heterogeneous growth hormone (GH) gene mutations in familial GH deficiency;Cogan;J. Clin. Endocrinol. Metab.,1993
5. Autosomal dominant growth hormone (GH) deficiency type II: the Del32-71-GH deletion mutant suppresses secretion of wild-type GH;Lee;Endocrinology,2000
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