Deletion of the paternal allele of the imprinted MEST/PEG1 region in a patient with Silver-Russell syndrome features
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2011.01719.x/fullpdf
Reference16 articles.
1. The endocrine phenotype in Silver-Russell syndrome is defined by the underlying epigenetic alteration.;Binder;J Clin Endocrinol Metab,2008
2. Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes.;Bartholdi;J Med Genet,2009
3. Epigenotype-phenotype correlation in Silver-Russell syndrome.;Wakeling;J Med Genet,2010
4. Segmental maternal UPD(7q) in Silver-Russell syndrome.;Eggermann;Clin Genet,2008
5. Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest.;Lefebvre;Nat Genet,1998
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