Growth Hormone Deficiency Type IB Caused by Cryptic Splicing of the GH-1 Gene
Author:
Publisher
Walter de Gruyter GmbH
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health
Link
https://www.degruyter.com/document/doi/10.1515/JPEM.2000.13.1.21/pdf
Reference15 articles.
1. Molecular basis for familial isolated growth hormone deficiency.
2. A new mutation causing inherited growth hormone deficiency: a compound heterozygote of a 6.7 kb deletion and a two base deletion in the third exon of the GH-1 gene
3. Isolated growth hormone (GH) deficiency type IA associated with a 45- kilobase gene deletion within the human GH gene cluster
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1. Growth Hormone-Releasing Hormone Receptor and Growth Hormone Gene Abnormalities;Growth Hormone Deficiency;2016
2. Combined effect of mutations of the GH1 gene and its proximal promoter region in a child with growth hormone neurosecretory dysfunction (GHND);Journal of Molecular Medicine;2007-05-04
3. Growth Hormone Deficiency Disorders;Principles of Molecular Medicine;2006
4. Alteraciones genéticas en los déficit de hormona del crecimiento;Anales de Pediatría Continuada;2004-01
5. Bases Genéticas dos Distúrbios de Crescimento;Arquivos Brasileiros de Endocrinologia & Metabologia;2002-08
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