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See Latest ArticlesExpanding the Spectrum of Mutations in GH1 and GHRHR: Genetic Screening in a Large Cohort of Patients with Congenital Isolated Growth Hormone Deficiency
Journal of Clinical Endocrinology and Metabolism, 07/02/09
Dattani M et al. - IGHD patients with severe growth failure and a positive family history should be screened for genetic mutations; the evolving endocrinopathy observed in some of these patients suggests the need for long-term follow-up.
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Depressive tendency in children with growth hormone deficiency
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A Molecular Basis for Variation in Clinical Severity of Isolated Growth Hormone Deficiency Type II
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Today in Basic Science/Genetics...keeping you current
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Lapatinib Plus Capecitabine Resolved Human Epidermal Growth Factor Receptor 2-Positive Brain Metastases
American Journal of Therapeutics, 12/04/09
Increased mRNA expression of collagen V gene in pulmonary fibrosis of systemic sclerosis
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Molecular Genomic Approaches to Infectious Diseases in Resource-Limited Settings
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Today in Endocrinology...keeping you current
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Muscular Strength Is Inversely Related to Prevalence and Incidence of Obesity in Adult Men
Obesity, 12/04/09
Lithium and thyroid
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