Publisher: John Wiley & Sons Inc
E-ISSN: 1552-4833|176|2|404-408
ISSN: 1552-4825
Source: American Journal Of Medical Genetics Part A, Vol.176, Iss.2, 2018-02, pp. : 404-408
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
Related content
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. :
Mutations in CDK5RAP2 cause Seckel syndrome
Molecular Genetics & Genomic Medicine, Vol. 2324-9269, Iss. 5, 2015-09 ,pp. :
Mutations in
Molecular Genetics & Genomic Medicine, Vol. 3, Iss. 5, 2015-09 ,pp. :
MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome
By Wan M.
Human Molecular Genetics, Vol. 10, Iss. 10, 2001-05 ,pp. :