Ngā hua rapu - D A Nickerson
- E whakaatu ana i te 1 - 5 hua o te 5
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Novel rare variants in congenital cardiac arrhythmia genes are frequent in drug-induced torsades de pointes mā Andrea H. Ramirez, Christian M. Shaffer, Jessica Delaney, David Sexton, Shawn Levy, Mark J. Rieder, D A Nickerson, Alfred L. George, D M Roden
I whakaputaina 2012Artigo -
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A new congenital disorder of glycosylation caused by a mutation in SSR4, the signal sequence receptor 4 protein of the TRAP complex mā Marie‐Estelle Losfeld, Bobby G. Ng, Martin Kircher, Kati J. Buckingham, Emily H. Turner, Alexey M. Eroshkin, Joshua D. Smith, Jay Shendure, D. A. Nickerson, Michael J. Bamshad, Hudson H. Freeze
I whakaputaina 2013Artigo -
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Recurrent de novo mutations implicate novel genes underlying simplex autism risk mā Brian J. O’Roak, Holly A.F. Stessman, Evan A. Boyle, Kali Witherspoon, Beth Martin, C. Lee, Laura Vives, Carl Baker, Joseph B. Hiatt, D. A. Nickerson, Raphael Bernier, Jay Shendure, Evan E. Eichler
I whakaputaina 2014Artigo -
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Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting mā LV Kalman, José A. G. Agúndez, Malin Lindqvist Appell, J.H. Black, GC Bell, Sotiria Boukouvala, Carsten Bruckner, Elspeth A. Bruford, KE Caudle, SA Coulthard, Ann K. Daly, AL Del Tredici, Johan T. den Dunnen, Katarzyna Drozda, Robin E. Everts, David A. Flockhart, Robert R. Freimuth, Andrea Gaedigk, Houda Hachad, Toinette Hartshorne, Magnus Ingelman‐Sundberg, Teri E. Klein, Volker M. Lauschke, DR Maglott, HL McLeod, GA McMillin, Meyer Ua, Müller Dj, D. A. Nickerson, WS Oetting, MA Pacanowski, Pratt Vm, MV Relling, Angharad M. Roberts, Rubinstein Ws, Katrin Sangkuhl, Matthias Schwab, Stuart A. Scott, SC Sim, RK Thirumaran, LH Toji, Rachel F. Tyndale, RHN van Schaik, Michelle Whirl‐Carrillo, K. L. B. Yeo, UM Zanger
I whakaputaina 2015Revisão
Ngā utauta rapu:
Ngā marau whai pānga
Biology
Gene
Genetics
Medicine
Mutation
Computational biology
Molecular biology
Phenotype
Autism
Autism spectrum disorder
Botany
Candidate gene
Cardiology
Chemical nomenclature
Chemistry
Computer network
Computer science
Computer security
Confusion
DNA
Drug
Genetic heterogeneity
Genotype
Glycosylation
Heritability of autism
Internal medicine
Locus (genetics)
Long QT syndrome
Microcephaly
Missense mutation