Author:
Pinnapureddy Ashish R.,Stayner Cherie,McEwan John,Baddeley Olivia,Forman John,Eccles Michael R.
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Genetics(clinical),General Medicine
Reference65 articles.
1. Barnetche T, Gourraud PA, Cambon-Thomsen A. Strategies in analysis of the genetic component of multifactorial diseases; biostatistical aspects. Transpl Immunol. 2005;14:255–66.
2. Thorisson GA, Smith AV, Krishnan L, Stein LD. The International HapMap Project Web site. Genome Res. 2005;15:1592–3.
3. McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine (Baltimore MD). Online Mendelian Inheritance of Man, OMIM®. http://www.ncbi.nlm.nih.gov/omim ). Accessed 21 March 2014.
4. Maxmen A. Exome sequencing deciphers rare diseases. Cell. 2011;144:635–7.
5. Gahl WA, Markello TC, Toro C, Fajardo KF, Sincan M, Gill F, et al. The national institutes of health undiagnosed diseases program: insights into rare diseases. Genet Med. 2012;14:51–9.
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