Verification of a Financial Instrument Allowing Rules-Based Pre-Acceptance Use of the Financial Instrument von MAGERS JAMES G, MCCOY RANDAL A

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Verification of a financial instrument allowing rules-based pre-acceptance use of the financial instrument von MAGERS JAMES G, MCCOY RANDAL A

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Verification of a financial instrument allowing rules-based pre-acceptance use of the financial instrument von McCoy, Randal A, Magers, James G

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Verification of a financial instrument using a random number of transactions von MAGERS JAMES G, MCCOY RANDAL A

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Verifying a financial instrument using a customer requested transaction von MAGERS JAMES G, WARD CHERYL L, MCCOY RANDAL A

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Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice von Farrow, Emily G, Yu, Xijie, Summers, Lelia J, Davis, Siobhan I, Fleet, James C, Allen, Matthew R, Robling, Alexander G, Stayrook, Keith R, Jideonwo, Victoria, Magers, Martin J, Garringer, Holly J, Vidal, Ruben, Chan, Rebecca J, Goodwin, Charles B, Hui, Siu L, Peacock, Munro, White, Kenneth E

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Hemorrhage Rates From Brain Arteriovenous Malformation in Patients With Hereditary Hemorrhagic Telangiectasia von Kim, Helen, Nelson, Jeffrey, Krings, Timo, terBrugge, Karel G, McCulloch, Charles E, Lawton, Michael T, Young, William L, Faughnan, Marie E, Chakinala, Murali, Gossage, James R, Henderson, Katharine, Iyer, Vivek, Kasthuri, Raj, Lin, Doris, Mager, Johannes Jurgen, McWilliams, Justin, McDonald, Jamie, Pawlikowska, Ludmila, Pollak, Jeffrey, Ratjen, Felix, Swanson, Karen, Vethanayagam, Dilini, White, Andrew, White, Robert I, Wilcox, Pearce

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The ACVRL1 c.314-35A>G polymorphism is associated with organ vascular malformations in hereditary hemorrhagic telangiectasia patients with ENG mutations, but not in patients with A... von Pawlikowska, Ludmila, Nelson, Jeffrey, Guo, Diana E., McCulloch, Charles E., Lawton, Michael T., Young, William L., Kim, Helen, Faughnan, Marie E.

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Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice von Farrow, Emily G., Yu, Xijie, Summers, Lelia J., Davis, Siobhan I., Fleet, James C., Allen, Matthew R., Robling, Alexander G., Stayrook, Keith R., Jideonwo, Victoria, Magers, Martin J., Garringer, Holly J., Vidal, Ruben, Chan, Rebecca J., Goodwin, Charles B., Hui, Siu L., Peacock, Munro, White, Kenneth E.

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