A human laterality disorder associated with a homozygous WDR16 deletion.

Autor: Ta-Shma, Asaf1, Perles, Zeev1, Yaacov, Barak2, Werner, Marion2, Frumkin, Ayala2, Rein, Azaria JJT1, Elpeleg, Orly2
Zdroj: European Journal of Human Genetics. Sep2015, Vol. 23 Issue 9, p1262-1265. 4p.
Databáze: Academic Search Ultimate