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Is maternal duplication of 11p15 associated with Silver-Russell syndrome? | Journal of Medical Genetics
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JPM | Free Full-Text | Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver–Russell Syndrome
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Clinical profile of a cohort of Silver-Russell syndrome patients followed at the Hospital Infantil de México Federico Gómez from 1998 to 2012 | Boletín Médico del Hospital Infantil de México (English Edition)
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12q14.3 microdeletion involving HMGA2 gene cause a Silver-Russell syndrome-like phenotype: a case report and review of the literature | springermedizin.de
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Novel mutation points to a hot spot in CDKN1C causing Silver–Russell syndrome | Clinical Epigenetics | Full Text
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Syndrome de Silver-Russell et syndrome de Temple : nouvelles avancées dans l'élucidation des mécanismes épigénétiques impliqués dans la croissance fœtale
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Frontiers | Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes
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Broad Clinical Spectrum in Silver-Russell Syndrome and Consequences for Genetic Testing in Growth Retardation | Semantic Scholar
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The Silver-Russell syndrome in the patient T. I. showing kypho-lordosis... | Download Scientific Diagram
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Hypomethylation of the H19 Gene Causes Not Only Silver-Russell Syndrome (SRS) but Also Isolated Asymmetry or an SRS-Like Phenotype - ScienceDirect
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Silver-Russell Syndrome-like Features in a Patient Carrying a Novel NF1 Mutation | Pediatric Research
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Prevalence and management of gastrointestinal manifestations in Silver– Russell syndrome | Archives of Disease in Childhood
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Figure 1 from Silver-Russell Syndrome - Part I: Clinical Characteristics and Genetic Background. | Semantic Scholar
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