Search Results - HENDRICKSON, Brant C

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  1. 1
    Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens

    Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens by Sugarman, Elaine A, Nagan, Narasimhan, Zhu, Hui, Akmaev, Viatcheslav R, Zhou, Zhaoqing, Rohlfs, Elizabeth M, Flynn, Kerry, Hendrickson, Brant C, Scholl, Thomas, Sirko-Osadsa, Deborah Alexa, Allitto, Bernice A

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  2. 2
    Multiple Rare Nonsynonymous Variants in the Adenomatous Polyposis Coli Gene Predispose to Colorectal Adenomas

    Multiple Rare Nonsynonymous Variants in the Adenomatous Polyposis Coli Gene Predispose to Colorectal Adenomas by AZZOPARDI, Duncan, DALLOSSO, Anthony R, WENSTRUP, Richard, SCHOLL, Thomas, CHEADLE, Jeremy P, ELIASON, Kristilyn, HENDRICKSON, Brant C, JONES, Natalie, RAWSTORNE, Edward, COLLEY, James, MOSKVINA, Valentina, FRYE, Cynthia, SAMPSON, Julian R

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  3. 3
    Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutations

    Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutations by JUDKINS, Thaddeus, HENDRICKSON, Brant C, DEFFENBAUGH, Amie M, ELIASON, Kristilyn, LECLAIR, Benoit, NORTON, Michael J, WARD, Brian E, PRUSS, Dmitri, SCHOLL, Thomas

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  4. 4
    Bioinformatics and Human Identification in Mass Fatality Incidents: The World Trade Center Disaster

    Bioinformatics and Human Identification in Mass Fatality Incidents: The World Trade Center Disaster by Leclair, Benoît, Shaler, Robert, Carmody, George R., Eliason, Kristilyn, Hendrickson, Brant C., Judkins, Thad, Norton, Michael J., Sears, Christopher, Scholl, Tom

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  5. 5
    Prevalence of five previously reported and recurrent BRCA1 genetic rearrangement mutations in 20,000 patients from hereditary breast/ovarian cancer families

    Prevalence of five previously reported and recurrent BRCA1 genetic rearrangement mutations in 20,000 patients from hereditary breast/ovarian cancer families by Hendrickson, Brant C., Judkins, Thaddeus, Ward, Benjamin D., Eliason, Kristilyn, Deffenbaugh, Amie E., Burbidge, Lynn Anne, Pyne, Kristin, Leclair, Benoît, Ward, Brian E., Scholl, Thomas

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  6. 6
    Single nucleotide polymorphisms in clinical genetic testing: the characterization of the clinical significance of genetic variants and their application in clinical research for BRCA1

    Single nucleotide polymorphisms in clinical genetic testing: the characterization of the clinical significance of genetic variants and their application in clinical research for BR... by Judkins, T, Hendrickson, B C, Deffenbaugh, A M, Scholl, T

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  7. 7
    Accurate STR Allele Designations at the FGA and vWA Loci Despite Primer Site Polymorphisms

    Accurate STR Allele Designations at the FGA and vWA Loci Despite Primer Site Polymorphisms by Hendrickson, BC, Leclair, B, Forrest, S, Ryan, J, Ward, BE, Petersen, D, Kupferschmid, TD, Scholl, T

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  8. 8
    Resolution of Individual Component Fluorescence Lifetimes from a Mixture of Trapped Ions by Laser-Induced Fluorescence/Ion Cyclotron Resonance

    Resolution of Individual Component Fluorescence Lifetimes from a Mixture of Trapped Ions by Laser-Induced Fluorescence/Ion Cyclotron Resonance by Cage, Brant, McFarland, Melinda A, Hendrickson, Christopher L, Dalal, Naresh S, Marshall, Alan G

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