Segmental maternal UPD(7q) in Silver-Russell syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2008.01057.x/fullpdf
Reference19 articles.
1. Use of multiple ligation-dependent probe amplification in Silver-Russell syndrome;Eggermann;Clin Genet,2008
2. The endocrine phenotype in Silver-Russell syndrome is defined by the underlying epigenetic alteration;Binder;J Clin Endocrinol Metab,2008
3. Chromosome 7p disruptions in Silver-Russell syndrome: delineating an imprinted candidate gene region;Monk;Hum Genet,2002
4. Is maternal duplication 11p15 associated with Silver-Russell syndrome?;Eggermann;J Med Genet,2005
5. A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region;Hannula;Am J Hum Genet,2001
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