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Publications

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Filters: Keyword is DNA Mutational Analysis  [Clear All Filters]
2015
Quantitative autofluorescence as a clinical tool for expedited differential diagnosis of retinal degeneration., Marsiglia, Marcela, Lee Winston, Mahajan Vinit B., Zernant Jana, Delori François C., Tsang Stephen H., and Sparrow Janet R. , JAMA Ophthalmol, 2015 Feb, Volume 133, Issue 2, p.219-20, (2015)
2010
Collagen XVIII mutation in Knobloch syndrome with acute lymphoblastic leukemia., Mahajan, Vinit B., Olney Ann Haskins, Garrett Penny, Chary Ajit, Dragan Ecaterina, Lerner Gary, Murray Jeffrey, and Bassuk Alexander G. , American journal of medical genetics. Part A, 2010 Nov, Volume 152A, Issue 11, p.2875-9, (2010)
2007
Transgenic mice carrying the H258N mutation in the gene encoding the beta-subunit of phosphodiesterase-6 (PDE6B) provide a model for human congenital stationary night blindness., Tsang, Stephen H., Woodruff Michael L., Jun Lin, Mahajan Vinit, Yamashita Clyde K., Pedersen Robert, Lin Chyuan-Sheng, Goff Stephen P., Rosenberg Thomas, Larsen Michael, et al. , Human mutation, 2007 Mar, Volume 28, Issue 3, p.243-54, (2007)