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Biochemistry|June 26, 1992
1H NMR and NOE studies of the purple acid phosphatases from porcine uterus and bovine spleenZ Wang, L J Ming, L Que, et al.Proceedings of the National Academy of Sciences of the United States of America|April 13, 2000
Reversal of charge selectivity in transmembrane protein pores by using noncovalent molecular adaptersL Q Gu, M Dalla Serra, J B Vincent, et al.American Journal of Human Genetics|July 13, 2000
Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individualJ B Vincent, J A Herbrick, H M Gurling, et al.Clinical Genetics|October 18, 2016
Biallelic truncating SCN9A mutation identified in four families with congenital insensitivity to pain from PakistanH A Sawal, R Harripaul, A Mikhailov, et al.Molecular Psychiatry|July 1, 1996
Point mutation analysis of the FMR-1 gene in autismJ B Vincent, D S Konecki, E Munstermann, et al.Journal of Biological Inorganic Chemistry : JBIC : a Publication of the Society of Biological Inorganic Chemistry|July 27, 2001
The trail of chromium(III) in vivo from the blood to the urine: the roles of transferrin and chromodulinB J Clodfelder, J Emamaullee, D D Hepburn, et al.Clinical Genetics|November 19, 2011
Identification of genomic deletions spanning the PCDH19 gene in two unrelated girls with intellectual disability and seizuresA K Vincent, A Noor, A Janson, et al.Molecular Psychiatry|July 8, 1999
Analysis of genome-wide CAG/CTG repeats, and at SEF2-1B and ERDA1 in schizophrenia and bipolar affective disorderJ B Vincent, A Petronis, E Strong, et al.The American Journal of Psychiatry|January 19, 1999
Genetic association analysis of serotonin system genes in bipolar affective disorderJ B Vincent, M Masellis, J Lawrence, et al.American Journal of Human Genetics|March 20, 2001
Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndromeE Petek, C Windpassinger, J B Vincent, et al.Pageof 8