Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues-Reference-Cited by-同舟云学术

Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues

Published:2010-07-22 Issue:1 Volume:80 Page:83-88
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Begemann M,Spengler S,Kanber D,Haake A,Baudis M,Leisten I,Binder G,Markus S,Rupprecht T,Segerer H,Fricke-Otto S,Mühlenberg R,Siebert R,Buiting K,Eggermann T

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2010.01514.x/fullpdf

Reference25 articles.

1. Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver-Russell syndrome.;Eggermann;Clin Genet,2008

2. Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver-Russell syndrome.;Bullman;J Med Genet,2008

3. The centromeric 11p15 imprinting centre is also involved in Silver-Russell syndrome.;Schönherr;J Med Genet,2007

4. Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome.;Cooper;Eur J Hum Genet,2005

5. Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells.;Bliek;Eur J Hum Genet,2009

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