Citations for
1IH, SRS11
IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasia.
Zeschnigk M, Albrecht B, Buiting K, Kanber D, Eggermann T, Binder G, Gromoll J, Prott EC, Seland S, Horsthemke B.
Eur J Hum Genet 16(3):328-34. Epub 2008 Jan 9. 2008
2H19, IH
Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype.
Bliek J, Terhal P, van den Bogaard MJ, Maas S, Hamel B, Salieb-Beugelaar G, Simon M, Letteboer T, van der Smagt J, Kroes H, Mannens M.
Am J Hum Genet 78(4):604-14. Epub 2006 Mar 1. 2006
3H19, IGF2, IH
Constitutional UPD for chromosome 11p15 in individuals with isolated hemihyperplasia is associated with high tumor risk and occurs following assisted reproductive technologies.
Shuman C, Smith AC, Steele L, Ray PN, Clericuzio C, Zackai E, Parisi MA, Meadows AT, Kelly T, Tichauer D, Squire JA, Sadowski P, Weksberg R.
Am J Med Genet A 140(14):1497-503. 2006
4H19, IH, KCNQ1OT1
LIT1 and H19 methylation defects in isolated hemihyperplasia.
Martin RA, Grange DK, Zehnbauer B, Debaun MR.
Am J Med Genet A 134(2):129-31. 2005
5BWS, H19, IH
Children with idiopathic hemihypertrophy and beckwith-wiedemann syndrome have different constitutional epigenotypes associated with wilms tumor.
Niemitz EL, Feinberg AP, Brandenburg SA, Grundy PE, Debaun MR.
Am J Hum Genet 77(5):887-91. Epub 2005 Oct 3. 2005