DOI:
10.1055/s-00029025
Journal of Pediatric Epilepsy
LinksClose Window
References
Elghezal H, Hannachi H, Mougou S, Kammoun H, Triki C, Saad A.
Ring chromosome 20 syndrome without deletions of the subtelomeric and CHRNA4—KCNQ2 genes loci.
Eur J Med Genet 2007;
50 (6) 441-445
Search in:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.