A Family with Mental Retardation, Epilepsy and Cerebellar Hypoplasia Showing Linkage to Chromosome 20p11.21-q11.23

Publisher： Karger

E-ISSN： 1662-680x|6|1|18-22

ISSN： 1662-680x

Source： Case Reports in Neurology, Vol.6, Iss.1, 2014-01, pp. : 18-22

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

Inclusion Body Myopathy-Like Changes in a Family with Cerebellar Atrophy, Mental Retardation and Abnormal Pupils

By  

European Neurology, Vol. 56, Iss. 3, 2006-10 ,pp. : 172-174

Karger

Access to resources Recommend Favorite

Hereditary Cerebellar Ataxia with Peripheral Neuropathy and Mental Retardation

By  

European Neurology, Vol. 43, Iss. 2, 2000-02 ,pp. : 82-87

Karger

Access to resources Recommend Favorite

Candidate genes showing no evidence for association or linkage with Alzheimer's disease using family-based methodologies

By Bertram L.   Blacker D.   Crystal A.   Mullin K.   Keeney D.   Jones J.   Basu S.   Yhu S.   Guenette S.   McInnis M.   Go R.   Tanzi R.  

Experimental Gerontology, Vol. 35, Iss. 9, 2000-12 ,pp. : 1353-1361

Elsevier

Access to resources Recommend Favorite

Genetic Linkage and Association Analysis of COPD-Related Traits on Chromosome 8p

By Hersh Craig   DeMeo Dawn   Raby Benjamin   Litonjua Augusto   Sylvia Jody   Sparrow David   Reilly John   Silverman Edwin  

COPD: Journal of Chronic Obstructive Pulmonary Disease, Vol. 3, Iss. 4, 2006-12 ,pp. : 189-194

Informa Healthcare

Access to resources Recommend Favorite

Cytogenetic and Immunohistochemical Characterization of Fragile X Syndrome in a Kuwaiti Family: Rapid Antibody Test for the Diagnosis of Mental Retardation Patients

By  

Medical Principles and Practice, Vol. 10, Iss. 2, 2001-07 ,pp. : 73-78

Karger

Access to resources Recommend Favorite