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

Publisher： Karger

E-ISSN： 1661-8777|2|3-5|213-216

ISSN： 1661-8769

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

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Mutations in epilepsy and intellectual disability genes in patients with features of Rett syndrome

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 9, 2015-09 ,pp. : 2017-2025

John Wiley & Sons Inc

Access to resources Recommend Favorite

Maternal uniparental isodisomy (iUPD) of chromosome 4 in a subject with mild intellectual disability and speech delay

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 9, 2015-09 ,pp. : 2219-2222

John Wiley & Sons Inc

Access to resources Recommend Favorite

Interstitial 1q21.1 Microdeletion Is Associated with Severe Skeletal Anomalies, Dysmorphic Face and Moderate Intellectual Disability

By  

Molecular Syndromology, Vol. 7, Iss. 6, 2016-10 ,pp. : 344-348

Karger

Access to resources Recommend Favorite

CNKSR2 deletions: A novel cause of X‐linked intellectual disability and seizures

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 7, 2015-07 ,pp. : 1668-1670

John Wiley & Sons Inc

Access to resources Recommend Favorite

Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 Deletions

By  

Molecular Syndromology, Vol. 5, Iss. 2, 2014-01 ,pp. : 57-64

Karger

Access to resources Recommend Favorite