Regulation of retinal progenitor expansion by Frizzled receptors: implications for microphthalmia and retinal coloboma

By Liu Chunqiao   Bakeri Hirva   Li Tiansen   Swaroop Anand  

Human Molecular Genetics, Vol. 21, Iss. 8, 2012-04 ,pp. : 1848-1860

Oxford University Press

Access to resources Recommend Favorite

CHX10 mutations cause non-syndromic microphthalmia/anophthalmia in Arab and Jewish kindreds

By Bar-Yosef Udy   Abuelaish Izzeldin   Harel Tamar   Hendler Neta   Ofir Rivka   Birk Ohad  

Human Genetics, Vol. 115, Iss. 4, 2004-09 ,pp. : 302-309

Springer Publishing Company

Access to resources Recommend Favorite

Domain disruption and mutation of the bZIP transcription factor, MAF , associated with cataract, ocular anterior segment dysgenesis and coloboma

By Munier F.  

Human Molecular Genetics, Vol. 11, Iss. 1, 2002-01 ,pp. : 33-42

Oxford University Press

Access to resources Recommend Favorite

E-cadherin missense mutations, associated with hereditary diffuse gastric cancer (HDGC) syndrome, display distinct invasive behaviors and genetic interactions with the Wnt and Notch pathways in Drosophila epithelia

By Pereira Paulo S.   Teixeira Alexandra   Ferreira Paulo   Fernandes Joana   Oliveira Carla   Seruca Raquel   Suriano Gianpaolo   Casares Fernando  

Human Molecular Genetics, Vol. 15, Iss. 10, 2006-05 ,pp. : 1704-1712

Oxford University Press

Access to resources Recommend Favorite

Methods for minimizing the loss of genetic diversity in conserved populations with overlapping generations

By Nomura Tetsuro  

Conservation Genetics, Vol. 6, Iss. 5, 2005-09 ,pp. : 655-663

Springer Publishing Company

Access to resources Recommend Favorite