Relationship between phenotype and genotype in growth hormone insensitivity syndrome
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1999.tb14376.x/fullpdf
Reference13 articles.
1. The Little Women of Loja — Growth Hormone–Receptor Deficiency in an Inbred Population of Southern Ecuador
2. Growth hormone receptor deficiency in Ecuador: clinical and biochemical phenotype in two populations
3. Clinical features and endocrine status in patients with growth hormone insensitivity (Laron syndrome)
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1. Guidelines for Growth Hormone and Insulin-Like Growth Factor-I Treatment in Children and Adolescents: Growth Hormone Deficiency, Idiopathic Short Stature, and Primary Insulin-Like Growth Factor-I Deficiency;Hormone Research in Paediatrics;2016
2. Recombinant Human Insulin-Like Growth Factor-1 Treatment: Ready for Primetime;Endocrinology and Metabolism Clinics of North America;2009-09
3. Novel nonsense mutation (p.Y113X) in the human growth hormone receptor gene in a Brazilian patient with Laron syndrome;Arquivos Brasileiros de Endocrinologia & Metabologia;2008-11
4. Investigação de baixa estatura: aspectos clínicos, laboratoriais e moleculares da insensibilidade ao hormônio de crescimento;Arquivos Brasileiros de Endocrinologia & Metabologia;2008-08
5. Normal Growth Spurt and Final Height despite Low Levels of All Forms of Circulating Insulin-Like Growth Factor-I in a Patient with Acid-Labile Subunit Deficiency;Hormone Research in Paediatrics;2007
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