Characterization of a 8q21.11 Microdeletion Syndrome Associated with Intellectual Disability and a Recognizable Phenotype

Autor: Palomares, María1,2 mpalomares.hulp@salud.madrid.org, Delicado, Alicia2,3, Mansilla, Elena2,3, de Torres, María Luisa2,3, Vallespín, Elena1,2, Fernandez, Luis2,3, Martinez-Glez, Victor1,2, García-Miñaur, Sixto2,4, Nevado, Julián1,2, Simarro, Fernando Santos2,4, Ruiz-Perez, Victor L.2,5, Lynch, Sally Ann6, Sharkey, Freddie H.7, Thuresson, Ann-Charlotte8, Annerén, Göran8, Belligni, Elga F.9, Martínez-Fernández, María Luisa2,10, Bermejo, Eva2,10,11, Nowakowska, Beata12,13, Kutkowska-Kazmierczak, Anna12
Zdroj: American Journal of Human Genetics. Aug2011, Vol. 89 Issue 2, p295-301. 7p.
Databáze: Academic Search Ultimate