15q Maternal Duplication and Neurodevelopmental Disorders; UBE3A is the Key

Publisher： John Wiley & Sons Inc

E-ISSN： 1098-1004|36|7|iii-iii

ISSN： 1059-7794

Source： HUMAN MUTATION, Vol.36, Iss.7, 2015-07, pp. : iii-iii

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

15q11.2 Duplication Encompassing Only the UBE3A Gene Is Associated with Developmental Delay and Neuropsychiatric Phenotypes

By  

HUMAN MUTATION, Vol. 36, Iss. 7, 2015-07 ,pp. : 689-693

John Wiley & Sons Inc

Access to resources Recommend Favorite

The Role of Calcium-Dependent Gene Expression in Autism Spectrum Disorders: Lessons from MeCP2, Ube3a and Beyond

By  

Neurosignals, Vol. 18, Iss. 2, 2010-10 ,pp. : 72-81

Karger

Access to resources Recommend Favorite

Histone Lysine Methylation and Neurodevelopmental Disorders

By Kim Jeong-Hoon   Lee Jang Ho   Lee Im-Soon   Lee Sung Bae   Cho Kyoung Sang  

International Journal of Molecular Sciences, Vol. 18, Iss. 7, 2017-06 ,pp. : 1404-1404

MDPI

Access to resources Recommend Favorite

Focal dysplasia of the cerebral cortex and infantile spasms associated with somatic 1q21.1‐q44 duplication including the AKT3 gene

By  

CLINICAL GENETICS, Vol. 88, Iss. 3, 2015-09 ,pp. : 241-247

John Wiley & Sons Inc

Access to resources Recommend Favorite

Targeted next‐generation sequencing in the diagnosis of neurodevelopmental disorders

By  

CLINICAL GENETICS, Vol. 88, Iss. 3, 2015-09 ,pp. : 288-292

John Wiley & Sons Inc

Access to resources Recommend Favorite