Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition von Davey, K M, Parboosingh, J S, McLeod, D R, Chan, A, Casey, R, Ferreira, P, Snyder, F F, Bridge, P J, Bernier, F P

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The T-786→C Mutation in Endothelial Nitric Oxide Synthase Is Associated With Hypertension von Hyndman, Matthew E, Parsons, Howard G, Verma, Subodh, Bridge, Peter J, Edworthy, Steven, Jones, Charlotte, Lonn, Eva, Charbonneau, Francois, Anderson, Todd J

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No Evidence of False Reassurance among Women with an Inconclusive BRCA1/2 Genetic Test Result von DORVAL, Michel, GAUTHIER, Geneviève, SIMARD, Jacques, MAUNSELL, Elizabeth, DUGAS, Michel J, ROULEAU, Isabelle, CHIQUETTE, Jocelyne, PLANTE, Marie, LAFRAMBOISE, Rachel, GAUDET, Michel, BRIDGE, Peter J

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Effect of heterozygosity for the methionine synthase 2756 A→G mutation on the risk for recurrent cardiovascular events von Hyndman, M.Eric, Bridge, Peter J., Warnica, J.Wayne, Fick, Gordon, Parsons, Howard G.

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Identification of Archaeological Animal Bone by PCR/DNA Analysis von Newman, Margaret E., Parboosingh, Jillian S., Bridge, Peter J., Ceri, Howard

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Disseminated bacille Calmette-Guérin infection in an infant with a novel deletion in the interferon-gamma receptor gene [Case Study] von CUNNINGHAM, J. A, KELLNER, J. D, BRIDGE, P. J, TREVENEN, C. L, MCLEOD, D. R, DAVIES, H. D

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Cost analysis of DNA-based testing in a large Canadian family with multiple endocrine neoplasia type 2 von Gilchrist, DM, Morrish, DW, Bridge, PJ, Brown, JL

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Genetic technologies, health care policy and the patent bargain von Caulfield, TA, Knoppers, BM, Gold, ER, Sheremeta, LE, Bridge, PJ

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Evaluation of the Quantase™ neonatal immunoreactive trypsinogen (IRT) screening assay for cystic fibrosis von Ball, Cindy L., Montgomery, Mark D., Bridge, Peter J., Lyon, Martha E.

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Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human gene von Koeberl, D D, Bottema, C D, Ketterling, R P, Bridge, P J, Lillicrap, D P, Sommer, S S

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Further evidence for genetic heterogeneity in familial hemophagocytic lymphohistiocytosis (FHLH) von Graham, G E, Graham, L M, Bridge, P J, Maclaren, L D, Wolff JEA, Coppes, M J, Egeler, R M

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Immunological and DNA Analysis of Blood Residues from a Surgeon's Kit used in the American Civil War von Newman, Margaret E., Byrne, Greg, Ceri, Howard, Dimnik, Leo S., Bridge, Peter J.

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Carrier detection and prenatal diagnosis of Pelizaeus-Merzbacher disease using a combination of anonymous DNA polymorphisms and the proteolipid protein (PLP) gene cDNA von Bridge, Peter J., MacLeod, Patrick M., Lillicrap, David P.

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An A to T transversion at position −5 of the Factor IX promoter results in hemophilia B von Picketts, David J., D'Souza, Cynthia, Bridge, Peter J., Lillicrap, David

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Maternal uniparental heterodisomy for chromosome 16: Case report von Woo, V., Bridge, P. J., Bamforth, J. S.

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Cosegregation of von Willebrand factor gene polymorphisms and possible germinal mosaicism in type IIB von Willebrand disease von Murray, EW, Giles, AR, Bridge, PJ, Peake, IR, Lillicrap, DP

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Cosegregation of von Willebrand Factor Gene Polymorphisms and Possible Germinal Mosaicism in Type IIB von Willebrand Disease von Murray, Elizabeth W., Giles, Alan R., Bridge, Peter J., Peake, lan R., Lillicrap, David P.

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Correction of the published sequence for the human proteolipid protein gene von WILKINS, P. J, D'SOUZA, C. R, BRIDGE, P. J

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The synthesis and composition of georgeite and its reactions to form other secondary copper(II) carbonates von Pollard, A. M., Thomas, R. G., Williams, P. A., Just, J., Bridge, P. J.

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Gonadal mosaicism in a family with adrenoleukodystrophy: Molecular diagnosis of carrier status among daughters of a gonadal mosaic when direct detection of the mutation is not poss... von Graham, G. E., MacLeod, P. M., Lillicrap, D. P., Bridge, P. J.

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