Genetic Disorders in the Growth Hormone – Insulin-Like Growth Factor-I Axis
Author:
Publisher
S. Karger AG
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health
Reference35 articles.
1. Characterization of the human growth hormone receptor gene and demonstration of a partial gene deletion in two patients with Laron-type dwarfism.
2. Deletions of the Homeobox GeneSHOX(Short Stature Homeobox) Are an Important Cause of Growth Failure in Children with Short Stature
3. A Novel Class of Pseudoautosomal Region 1 Deletions Downstream of SHOX Is Associated with Léri-Weill Dyschondrosteosis
4. Nonsense mutation in the human growth hormone-releasing hormone receptor causes growth failure analogous to the little (lit) mouse
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