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Dive into the research topics where Martin R Littlejohn is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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- 3 Article
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Comprehensive Mutation Analysis for Congenital Muscular Dystrophy: A Clinical PCR-Based Enrichment and Next-Generation Sequencing Panel
Valencia, C. A., Ankala, A., Rhodenizer, D., Bhide, S., Littlejohn, M. R., Keong, L. M., Rutkowski, A., Sparks, S., Bonnemann, C. & Hegde, M., Jan 17 2013, In: PloS one. 8, 1, e53083.Research output: Contribution to journal › Article › peer-review
Open Access61 Link opens in a new tab Scopus citations -
Assessment of target enrichment platforms using massively parallel sequencing for the mutation detection for congenital muscular dystrophy
Valencia, C. A., Rhodenizer, D., Bhide, S., Chin, E., Littlejohn, M. R., Keong, L. M., Rutkowski, A., Bonnemann, C. & Hegde, M., May 2012, In: Journal of Molecular Diagnostics. 14, 3, p. 233-246 14 p.Research output: Contribution to journal › Article › peer-review
Open Access48 Link opens in a new tab Scopus citations -
Immunohistochemical profile and fluorescence in situ hybridization analysis of diffuse large B-cell lymphoma in Northern China
Li, T., Medeiros, L. J., Lin, P., Yin, H., Littlejohn, M., Im, W., Lennon, P. A., Hu, P., Jorgensen, J. L., Liang, M., Guo, H. & Yin, C. C., May 2010, In: Archives of Pathology and Laboratory Medicine. 134, 5, p. 759-765 7 p.Research output: Contribution to journal › Article › peer-review
12 Link opens in a new tab Scopus citations