| 1 | IH, 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
|
| 2 | H19, 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
|
| 3 | H19, 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
|
| 4 | H19, 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
|
| 5 | BWS, 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
|