Developmental validation of the PowerPlex® Fusion System for analysis of casework and reference samples: A 24-locus multiplex for new database standards von Oostdik, Kathryn, Lenz, Kristy, Nye, Jeffrey, Schelling, Kristin, Yet, Donald, Bruski, Scott, Strong, Joshua, Buchanan, Clint, Sutton, Joel, Linner, Jessica, Frazier, Nicole, Young, Hays, Matthies, Learden, Sage, Amber, Hahn, Jeff, Wells, Regina, Williams, Natasha, Price, Monica, Koehler, Jody, Staples, Melisa, Swango, Katie L, Hill, Carolyn, Oyerly, Karen, Duke, Wendy, Katzilierakis, Lesley, Ensenberger, Martin G, Bourdeau, Jeanne M, Sprecher, Cynthia J, Krenke, Benjamin, Storts, Douglas R

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A quantitative PCR assay for the assessment of DNA degradation in forensic samples von Swango, Katie L., Timken, Mark D., Chong, Mavis Date, Buoncristiani, Martin R.

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Developmental validation of a multiplex qPCR assay for assessing the quantity and quality of nuclear DNA in forensic samples von Swango, Katie L, Hudlow, William R, Timken, Mark D, Buoncristiani, Martin R

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A quadruplex real-time qPCR assay for the simultaneous assessment of total human DNA, human male DNA, DNA degradation and the presence of PCR inhibitors in forensic samples: A diag... von Hudlow, William R, Chong, Mavis Date, Swango, Katie L, Timken, Mark D, Buoncristiani, Martin R

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Fine Mapping of the Human Biotinidase Gene and Haplotype Analysis of Five Common Mutations von Blanton, Susan Halloran, Pandya, Arti, Landa, Barbara L., Javaheri, Razieh, Xia, Xia-Juan, Nance, Walter E., Pomponio, Robert J., Norrgard, Karen J., Swango, Katie L., Demirkol, Mübeccel, Gülden, Hüner, Coskun, Turgay, Tokatli, Aysegül, Ozalp, Imran, Wolf, Barry

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Partial biotinidase deficiency is usually due to the D444H mutation in the biotinidase gene von SWANGO, K. L, DEMIRKOL, M, HÜNER, G, PRONICKA, E, SYKUT-CEGIELSKA, J, SCHULZE, A, WOLF, B

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Conservation of Biotindase in Mammals and Identification of the Putative Biotinidase Gene in Drosophila melanogaster von Swango, Katie L, Wolf, Barry

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Double mutation (A171T) and D444H) is a common cause of profound biotinidase deficiency in children ascertained by newborn screening in the United States von Norrgard, Karen J, Pomponio, Robert J, Swango, Katie L, Hymes, Jeanne, Reynolds, Thomas, Buck, Gregory A, Wolf, Barry

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Double mutation (A171T) and (D444H) is a common cause of profound biotinidase deficiency in children ascertained by newborn screening in the United States von Norrgard, Karen J., Pomponio, Robert J., Swango, Katie L., Hymes, Jeanne, Reynolds, Thomas, Buck, Gregory A., Wolf, Barry

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Mutation (Q456H) Is the Most Common Cause of Profound Biotinidase Deficiency in Children Ascertained by Newborn Screening in the United States von Norrgard, Karen J., Pomponio, Robert J., Swango, Katie L., Hymes, Jeanne, Reynolds, Thomas R., Buck, Gregory A., Wolf, Barry

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