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Submicroscopic genomic alterations in Silver-Russell syndrome and Silver-Russell-like patients
Journal of Medical Genetics, 09/25/09
Bruce S et al. – The authors found unexpected submicroscopic genomic events with pathogenic potential in three molecularly unexplained patients with mild SRS. The findings emphasize that SRS is heterogeneous in genetic etiology beyond the major groups of H19 hypomethylation and matUPD7 and that unbiased genome–scale screens may reveal novel genotype–phenotype correlations.
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Advances in fibromyalgia treatment: understanding endogenous pain modulation
International Journal of Clinical Rheumatology, 11/09/09
How triggers trigger acute migraine attacks: A hypothesis
Medical Hypotheses, 11/23/09
Functional activation of proline-rich tyrosine kinase2 (PYK2) in peripheral blood mononuclear cells from patients with systemic lupus erythematosus
BMC Musculoskeletal Disorders, 11/18/09
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