Author:
Greenblatt Marc S.,Brody Lawrence C.,Foulkes William D.,Genuardi Maurizio,Hofstra Robert M.W.,Olivier Magali,Plon Sharon E.,Sijmons Rolf H.,Sinilnikova Olga,Spurdle Amanda B.,
Subject
Genetics(clinical),Genetics
Reference40 articles.
1. Recommendations for a nomenclature system for human gene mutations;Antonarakis;Hum Mutat,1998
2. Novel biallelic mutations in MSH6 and PMS2 genes: gene conversion as a likely cause of PMS2 gene inactivation;Auclair;Hum Mutat,2007
3. Human variome microattribution reviews. [Editorial];Axton;Nat Genet,2008
4. Bell J, Bodmer D, Sistermans E, Ramsden SC. 2007. Practice guidelines for the interpretation and reporting of unclassified variants (UV) in clinical molecular genetics. UK Clinical Molecular Genetics Society Meeting Report. Clinical Molecular Genetics Society epublication. http://cmgsweb.shared.hosting.zen.co.uk/.
5. Interpreting missense variants: comparing computational methods in human disease genes CDKN2A, MLH1, MSH2, MECP2, and tyrosinase (TYR);Chan;Hum Mutat,2007
Cited by
39 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献