Familial Growth Hormone Deficiency and Mutations in the GHRH Receptor Gene

Keyphrases

• Receptor Gene 100%
• Releasing Hormone 100%
• Hormone Receptor 100%
• Growth Hormone Deficiency 100%
• GHRH Receptor 100%
• Isolated GH Deficiency 50%
• Growth Hormone 33%
• Receptor mutations 33%
• Anterior pituitary 33%
• Magnetic Resonance Imaging 16%
• Autosomal Recessive 16%
• First Year of Life 16%
• Growth Factors 16%
• Cell Surface Receptor 16%
• Insulin-like 16%
• Hypothalamus 16%
• Parental Consanguinity 16%
• Gene mutation 16%
• Biochemical Studies 16%
• Low Serum 16%
• Reduced Growth 16%
• Growth Failure 16%
• Hypoplasia 16%
• Common Cause 16%
• Compound Heterozygous mutation 16%
• Growth Hormone-releasing Hormone 16%
• Membrane Surface 16%
• Normal Weight 16%
• Growth Hormone Treatment 16%
• Kindred 16%
• Hormone Response 16%
• Hormone-related Genes 16%
• Weight at Birth 16%
• Deficiency Cases 16%
• Hypophyseal 16%

Neuroscience

• Somatotropic Cell 33%

Biochemistry, Genetics and Molecular Biology

• Somatotropic Cell 28%