Mild to Moderate Intellectual Disability and Significant Speech and Language Deficits in Patients with FOXP1 Deletions and Mutations

By  

Molecular Syndromology, Vol. 2, Iss. 3-5, 2011-08 ,pp. : 213-216

Karger

Access to resources Recommend Favorite

MECP2 mutations account for most cases of typical forms of Rett syndrome

By Bienvenu Thierry   Carrié Alain   de Nicolas  

Human Molecular Genetics, Vol. 9, Iss. 9, 2000-05 ,pp. : 1377-1384

Oxford University Press

Access to resources Recommend Favorite

Delineation of the KIAA2022 mutation phenotype: Two patients with X‐linked intellectual disability and distinctive features

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 6, 2015-06 ,pp. : 1349-1353

John Wiley & Sons Inc

Access to resources Recommend Favorite

Rett Syndrome

By  

Molecular Syndromology, Vol. 2, Iss. 3-5, 2012-04 ,pp. : 113-127

Karger

Access to resources Recommend Favorite

Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome

By Nuber Ulrike A.  

Human Molecular Genetics, Vol. 14, Iss. 15, 2005-08 ,pp. : 2247-2256

Oxford University Press

Access to resources Recommend Favorite