Two sisters with Silver-Russell phenotype
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference31 articles.
1. Autosomal dominant Russell-Silver syndrome;Al-Fifi;Am J Med Genet,1996
2. Clinical and molecular findings in two patients with Russell-Silver syndrome and UPD7: Comparison with non-UPD7 cases;Bernard;Am J Med Genet,1999
3. Asymmetrical dwarfism, or Silver's syndrome, in two male siblings;Callaghan;Med J Aust,1970
4. Deletion short arm 18 and Silver-Russell syndrome;Christensen;Acta Paediatr Scand,1978
5. Three-generation dominant transmission of the Silver-Russell syndrome;Duncan;Am J Med Genet,1990
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1. Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome: Opposite Phenotypes with Heterogeneous Molecular Etiology;Molecular Syndromology;2016
2. The Frequency of Methylation Abnormalities Among Estonian Patients Selected by Clinical Diagnostic Scoring Systems for Silver–Russell Syndrome and Beckwith–Wiedemann Syndrome;Genetic Testing and Molecular Biomarkers;2015-12
3. Epigenetic and genetic diagnosis of Silver–Russell syndrome;Expert Review of Molecular Diagnostics;2012-06
4. A distinctive autosomal recessive syndrome of severe disproportionate short stature with short long bones, brachydactyly, and hypotrichosis in two consanguineous Arab families;European Journal of Medical Genetics;2012-04
5. Genetics of Silver–Russell Syndrome;eLS;2012-02-15
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