Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference84 articles.
1. 11p15 ICR1 loss of methylation is a commonand specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations;Netchine;J. Clin. Endocrinol. Metab.,2007
2. Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver Russell syndrome;Gicquel;Nat. Genet.,2005
3. Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype;Bliek;Am. J. Hum. Genet.,2006
4. Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver-Russell syndrome;Eggermann;Clin. Genet.,2008
5. Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome;Cooper;Eur. J. Hum. Genet.,2005
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