Identifying Genes Responsible for Intellectual Disability in Consanguineous Families

Publisher： Karger

E-ISSN： 1423-0062|77|1-4|150-160

ISSN： 0001-5652

Source： Human Heredity, Vol.77, Iss.1-4, 2014-07, pp. : 150-160

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

MED23‐associated intellectual disability in a non‐consanguineous family

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 6, 2015-06 ,pp. : 1374-1380

John Wiley & Sons Inc

Access to resources Recommend Favorite

Novel sequence variants in the LIPH and LPAR6 genes underlies autosomal recessive woolly hair/hypotrichosis in consanguineous families

By  

CONGENITAL ANOMALIES, Vol. 58, Iss. 1, 2018-01 ,pp. : 24-28

John Wiley & Sons Inc

Access to resources Recommend Favorite

Dandy–Walker malformation, genitourinary abnormalities, and intellectual disability in two families

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 11, 2015-11 ,pp. : 2503-2507

John Wiley & Sons Inc

Access to resources Recommend Favorite

Homozygous 16p13.11 duplication associated with mild intellectual disability and urinary tract malformations in two siblings born from consanguineous parents

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 11, 2015-11 ,pp. : 2714-2719

John Wiley & Sons Inc

Access to resources Recommend Favorite

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