Hereditary isolated growth hormone deficiency caused by GH1 gene mutations in Japanese patients
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference23 articles.
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2. Molecular basis for familial isolated growth hormone deficiency;Phillips,1981
3. Pheno???ypc heterogeneity in familial isolated growth hormone deficiency (IGHD) type IA;Rivarola;J Clin En locrinol Metab,1984
4. Familial growth hormone deficiency resulting from a 7.6 kb deletion within the growth hormone gene cluster;Braga;Am J Med Genet,1986
5. Isolated growth hormone (GH) deficiency type IA associated with a double deletion in the human GH gene cluster;Goossens;J Clin Endocrinol Metab,1986
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1. Genetics of GHRH, GHRH-receptor, GH and GH-receptor: Its impact on pharmacogenetics;Best Practice & Research Clinical Endocrinology & Metabolism;2011-02
2. Genetic defects causing functional and structural isolated growth hormone deficiency;Translational Neuroscience;2011-01-01
3. Isolated growth hormone deficiency;Pituitary;2007-10-29
4. A case with isolated growth hormone deficiency caused by compound heterozygous mutations in GH-1: A novel missense mutation in the initiation codon and a 7.6kb deletion;Growth Hormone & IGF Research;2007-06
5. Genetics of Growth Hormone Deficiency;Endocrinology and Metabolism Clinics of North America;2007-03
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