David K Crockett

Multiple endocrine neoplasia type 2 RET protooncogene database: Repository of MEN2‐associated RET sequence variation and reference for genotype/phenotype correlations

Rong Mao, Carl T Wittwer, Rebecca L Margraf, 2009, Human mutation.

Consensus: a framework for evaluation of uncertain gene variants in laboratory test reporting

Joyce A. Mitchell, Elaine Lyon, Julio C Facelli, 2012, Genome Medicine.

Utility of characteristic QTOF MS/MS fragmentation for MHC class I peptides.

D. Crockett, P. Jensen, J. Delgado, 2011, Journal of proteome research.

Proteomic identification of oncogenic chromosomal translocation partners encoding chimeric anaplastic lymphoma kinase fusion proteins.

Alan L Rockwood, Kojo S J Elenitoba-Johnson, K. Elenitoba-Johnson, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Sequence alignment by cross-correlation.

Alan L Rockwood, Kojo S J Elenitoba-Johnson, David K Crockett, 2005, Journal of biomolecular techniques : JBT.

The Alport syndrome COL4A5 variant database

Kelli Sumner, Elaine Lyon, Genevieve Pont-Kingdon, 2010, Human mutation.

Mutation database for the galactose‐1‐phosphate uridyltransferase (GALT) gene

Rong Mao, A. Phansalkar, D. Crockett, 2007, Human mutation.