PARK2 Microduplication: Clinical and Molecular Characterization of a Further Case and Review of the Literature

Publisher： Karger

E-ISSN： 1661-8777|7|5|282-286

ISSN： 1661-8769

Source： Molecular Syndromology, Vol.7, Iss.5, 2016-09, pp. : 282-286

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

Clinical and molecular characterization of chromosome 7p22.1 microduplication detected by array CGH

By  

American Journal Of Medical Genetics Part A, Vol. 155, Iss. 10, 2011-10 ,pp. : 2508-2511

John Wiley & Sons Inc

Access to resources Recommend Favorite

Endocrinological Abnormalities Are a Main Feature of 17p13.1 Microduplication Syndrome: A New Case and Literature Review

By  

Molecular Syndromology, Vol. 7, Iss. 6, 2016-10 ,pp. : 337-343

Karger

Access to resources Recommend Favorite

Distal 7q11.23 Duplication, an Emerging Microduplication Syndrome: A Case Report and Further Characterisation

By  

Molecular Syndromology, Vol. 7, Iss. 5, 2016-08 ,pp. : 287-291

Karger

Access to resources Recommend Favorite

Pure duplication of 19p13.3 in three members of a family with intellectual disability and literature review. Definition of a new microduplication syndrome

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 7, 2015-07 ,pp. : 1614-1620

John Wiley & Sons Inc

Access to resources Recommend Favorite

Clinical and molecular delineation of Tetrasomy 9p syndrome: Report of 12 new cases and literature review

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 6, 2015-06 ,pp. : 1252-1261

John Wiley & Sons Inc

Access to resources Recommend Favorite