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The American Journal of Dermatopathology|March 25, 2008
Erythema nodosum in association with newly diagnosed hairy cell leukemia and group C streptococcus infectionRishi R Patel, Eugene B Kirkland, Dennis H Nguyen, et al.Proceedings of the National Academy of Sciences of the United States of America|April 25, 1995
Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy geneS Selig, S Bruno, J M Scharf, et al.Human Molecular Genetics|August 1, 1994
Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6pJ A Knowles, Y Shugart, P Banerjee, et al.The Journal of Investigative Dermatology|December 5, 2008
Hair follicle stem cell-specific PPARgamma deletion causes scarring alopeciaPratima Karnik, Zenar Tekeste, Thomas S McCormick, et al.Journal of the American Academy of Dermatology|December 19, 2006
A case of Churg-Strauss syndrome associated with antiphospholipid antibodiesKatalin Ferenczi, Timothy Chang, Melissa Camouse, et al.Frontiers in Neuroanatomy|November 28, 2014
Integration of multiscale dendritic spine structure and function data into systems biology modelsJames J Mancuso, Jie Cheng, Zheng Yin, et al.Neurology|December 17, 1998
Evaluation of the alpha(2A)-adrenergic receptor gene in a heritable form of temporal lobe epilepsyM H Wilson, R S Puranam, R Ottman, et al.Neurology|April 14, 2004
LGI1 mutations in autosomal dominant partial epilepsy with auditory featuresR Ottman, M R Winawer, S Kalachikov, et al.Annals of Neurology|July 1, 1997
Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologuesC H Wang, T A Carter, K Das, et al.Progress in Retinal and Eye Research|June 30, 2016
Structural and molecular bases of rod photoreceptor morphogenesis and diseaseTheodore G Wensel, Zhixian Zhang, Ivan A Anastassov, et al.Pageof 31