Author:
Boschann Felix,Fischer-Zirnsak Björn,Wienker Thomas F.,Holtgrewe Manuel,Seelow Dominik,Eichhorn Birgit,Döhnert Steffi,Fahsold Raimund,Horn Denise,Graul-Neumann Luitgard M.
Subject
Genetics(clinical),Genetics,General Medicine
Reference17 articles.
1. Deletions in the VPS13B (COH1) gene as a cause of Cohen syndrome;Balikova;Hum. Mutat.,2009
2. A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies;Cohen;J. Pediatr.,1973
3. Cohen syndrome is associated with major glycosylation defects;Duplomb;Hum. Mol. Genet.,2014
4. Integrated sequence analysis pipeline provides one-stop solution for identifying disease-causing mutations;Hu;Hum. Mutat.,2014
5. Craniofacial features in Cohen syndrome: an anthropometric and cephalometric analysis of 14 patients;Hurmerinta;Clin. Genet.,2002
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