DOI:
10.1055/s-00000140
Pädiatrie up2date
LinksClose Window
References
Kleefstra T, van Zelst-Stams WA, Nillesen WM et al.
Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype.
J Med Genet 2009;
46: 598-606
Access:
We do not assume any responsibility for the contents of the web pages of other providers.