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 |
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Zdroj: | European Journal of Human Genetics. Sep2015, Vol. 23 Issue 9, p1262-1265. 4p. |
Databáze: | Academic Search Ultimate |
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