Author： Bar-Yosef Udy Abuelaish Izzeldin Harel Tamar Hendler Neta Ofir Rivka Birk Ohad
Publisher： Springer Publishing Company
ISSN： 0340-6717
Source： Human Genetics, Vol.115, Iss.4, 2004-09, pp. : 302-309
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Related content
SHOX Haploinsufficiency as a Cause of Syndromic and Nonsyndromic Short Stature
Molecular Syndromology, Vol. 7, Iss. 1, 2016-03 ,pp. :
Access to resources
Recommend
By Froyen Guy Bauters Marijke Boyle Jackie Esch Hilde Govaerts Karen Bokhoven Hans Ropers Hans-Hilger Moraine Claude Chelly Jamel Fryns Jean-Pierre Marynen Peter Gecz Jozef Turner Gillian
Human Genetics, Vol. 121, Iss. 5, 2007-06 ,pp. :
Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome
By Williamson Kathleen A. Hever Ann M. Rainger Joe Rogers R. Curtis Magee Alex Fiedler Zdenek Keng Wee Teik Sharkey Freddie H. McGill Niolette Hill Clare J. Schneider Adele Messina Mario Turnpenny Peter D. Fantes Judy A. van Heyningen Veronica FitzPatrick David R.
Human Molecular Genetics, Vol. 15, Iss. 9, 2006-05 ,pp. :
Mutations in SOX2 cause anophthalmia–esophageal–genital (AEG) syndrome
By Williamson Kathleen A. Hever Ann M. Rainger Joe Rogers R. Curtis Magee Alex Fiedler Zdenek Keng Wee Teik Sharkey Freddie H. McGill Niolette Hill Clare J. Schneider Adele Messina Mario Turnpenny Peter D. Fantes Judy A. van Heyningen Veronica FitzPatrick David R.
Human Molecular Genetics, Vol. 15, Iss. 12, 2006-06 ,pp. :