Epigenetic and genetic diagnosis of Silver–Russell syndrome
Author:
Affiliation:
1. Institute of Human Genetics, University Hospital Aachen, Pauwelsstr. 30, D-52074 Aachen, Germany.
2. Institute of Human Genetics, University Hospital Aachen, Pauwelsstr. 30, D-52074 Aachen, Germany
Publisher
Informa UK Limited
Subject
Genetics,Molecular Biology,Molecular Medicine,Pathology and Forensic Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1586/erm.12.43
Reference57 articles.
1. The genetic aetiology of Silver-Russell syndrome
2. Cognitive development in Silver-Russell syndrome: a sibling-controlled study
3. 11p15 Imprinting Center Region 1 Loss of Methylation Is a Common and Specific Cause of Typical Russell-Silver Syndrome: Clinical Scoring System and Epigenetic-Phenotypic Correlations
4. Clinically Distinct Epigenetic Subgroups in Silver-Russell Syndrome: The Degree ofH19Hypomethylation Associates with Phenotype Severity and Genital and Skeletal Anomalies
5. Epigenotype-phenotype correlations in Silver-Russell syndrome
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