home : about us : ahead of print : current issue : archives search instructions : subscriptionLogin 
Users online: 1405      Small font sizeDefault font sizeIncrease font size Print this page Email this page

    Article Cited by others

CASE REPORT

Paternally derived translocation t(8;18)(q22.1;q22)pat associated in a patient with developmental delay: Case report and review

Rao Lakshmi, Kanakavalli Murthy, Padmalatha Venkata, Nallari Pratibha, Singh Lalji

Year : 2010| Volume: 5| Issue : 1 | Page no: 64-67

   This article has been cited by
 
1 HECT domain-containing E3 ubiquitin ligase NEDD4L negatively regulates Wnt signaling by targeting dishevelled for proteasomal degradation
Ding, Y. and Zhang, Y. and Xu, C. and Tao, Q.-H. and Chen, Y.-G.
Journal of Biological Chemistry. 2013; 288(12): 8289-8298
[Pubmed]  [Google Scholar]
2 Clinical and cytogenetic study of a case with familial chromosomal translocation presenting with facial dysmorphism and axial neuropathy
El-Bassyouni, H.T. and Shehab, M. and Kora, H.M. and Temtamy, S.A.
Genetic Counseling. 2012; 23(1): 41-50
[Pubmed]  [Google Scholar]

 

Read this article