loss-of-function mutations in developmental eye disorders including SHORT syndrome

Author: Reis Linda   Tyler Rebecca   Schilter Kala   Abdul-Rahman Omar   Innis Jeffrey   Kozel Beth   Schneider Adele   Bardakjian Tanya   Lose Edward   Martin Donna   Broeckel Ulrich   Semina Elena  

Publisher: Springer Publishing Company

ISSN: 0340-6717

Source: Human Genetics, Vol.130, Iss.4, 2011-10, pp. : 495-504

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

Related content