Molecular genetic screening of MBS1 locus on chromosome 13 for microdeletions and exclusion of FGF9, GSH1 and CDX2 as causative genes in patients with Moebius syndrome.
暂无分享,去创建一个
B. Tatlı | H. Kayserili | G. Toksoy | B. Karaman | Z. Uyguner | A. Yuksel | S. Candan | B. Geckinli | H. Eriş | S. Başaran | A. Uzumcu