Author:
Bruce Christopher K.,Smith Matthew,Rahman Fatima,Liu Zhi-feng,McMullan Dominic J.,Ball Sarah,Hartley Jane,Kroos Marian A.,Heptinstall Lesley,Reuser Arnold J.J.,Rolfs Arndt,Hendriksz Chris,Kelly Deirdre A.,Barrett Timothy G.,MacDonald Fiona,Maher Eamonn R.,Gissen Paul
Subject
Genetics (clinical),Genetics
Reference23 articles.
1. Molecular characterization of Neisseria meningitidis isolates using a resequencing DNA microarray;Corless;J Mol Diagn,2008
2. Mutations in VIPAR cause an arthrogryposis, renal dysfunction, and cholestatsis syndrome phenotype with defects in epithelial polarisation;Cullinane;Nat Genet,2010
3. Cullinane AR Straatman-Iwanowska A Zaucker A Wakabayash Y Bruce C Rahman F Rappoport J Arias IM Wolburg H Knisely AS Kelly DA Mueller F Maher ER Gissen P Mutations in polarin (PLRN) cause an ARC syndrome phenotype and defects in epithelial polarisation and apical junction complex formation (Abstract 290)
4. High-throughput variation detection and genotyping using microarrays;Cutler;Genome Res,2001
5. High throughput genetic analysis of congenital myasthenic syndromes using resequencing microarrays;Denning;PLoS One,2007
Cited by
16 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