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Atypical GH Insensitivity Syndrome and Severe Insulin-Like Growth Factor-I Deficiency Resulting from Compound Heterozygous Mutations of the GH Receptor, Including a Novel Frameshift Mutation Affecting the Intracellular Domain.
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- Hormone Research in Paediatrics, 2010, v. 74, n. 6, p. 406, doi. 10.1159/000314968
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- Article
Six Year Old with Autoimmune Polyglandular Syndrome: Can Genetics Tell Us the Story?
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- Journal of Pediatric Endocrinology & Metabolism, 2010, v. 23, n. 7, p. 725, doi. 10.1515/JPEM.2010.23.7.725
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- Publication type:
- Article
mTOR signaling contributes to chondrocyte differentiation.
- Published in:
- Developmental Dynamics, 2008, v. 237, n. 3, p. 702, doi. 10.1002/dvdy.21464
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- Article