Delineation of a de novo 7q21.3q31.1 Deletion by CGH-SNP Arrays in a Girl with Multiple Congenital Anomalies Including Severe Glaucoma

Publisher： Karger

E-ISSN： 1661-8777|4|6|285-291

ISSN： 1661-8769

Source： Molecular Syndromology, Vol.4, Iss.6, 2013-07, pp. : 285-291

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

A 10q21.3q22.2 microdeletion identified in a patient with severe developmental delay and multiple congenital anomalies including congenital heart defects

By  

CONGENITAL ANOMALIES, Vol. 58, Iss. 1, 2018-01 ,pp. : 36-38

John Wiley & Sons Inc

Access to resources Recommend Favorite

De novo 4q duplication/deletion in a fetus with a congenital heart defect

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 8, 2015-08 ,pp. : 1932-1936

John Wiley & Sons Inc

Access to resources Recommend Favorite

Language Impairment Resulting from a de novo Deletion of 7q32.1q33

By  

Molecular Syndromology, Vol. 7, Iss. 5, 2016-08 ,pp. : 292-298

Karger

Access to resources Recommend Favorite

Severe Progressive Autism Associated with Two de novo Changes: A 2.6-Mb 2q31.1 Deletion and a Balanced t(14;21)(q21.1;p11.2) Translocation with Long-Range Epigenetic Silencing of LRFN5 Expression

By  

Molecular Syndromology, Vol. 1, Iss. 1, 2010-02 ,pp. : 46-57

Karger

Access to resources Recommend Favorite

Interstitial deletion 5q14.3q21.3 associated with lethal epilepsy

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 4, 2015-04 ,pp. : 866-871

John Wiley & Sons Inc

Access to resources Recommend Favorite