Search Results - LIBURD, Nikki

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  1. 1
    Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29

    Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29 by Wilcox, Edward R, Burton, Quianna L, Naz, Sadaf, Riazuddin, Saima, Smith, Tenesha N, Ploplis, Barbara, Belyantseva, Inna, Ben-Yosef, Tamar, Liburd, Nikki A, Morell, Robert J, Kachar, Bechara, Wu, Doris K, Griffith, Andrew J, Riazuddin, Sheikh, Friedman, Thomas B

    Published in Cell
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  2. 2
    Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome

    Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome by LIBURD, Nikki, GHOSH, Manju, SMITH, Ann C. M, CHEN, Ken-Shiung, LUPSKI, James R, WILCOX, Edward R, POTOCKI, Lorraine, FRIEDMAN, Thomas B, RIAZUDDIN, Saima, NAZ, Sadaf, KHAN, Shaheen, AHMED, Zubair, RIAZUDDIN, Sheikh, YONG LIANG, MENON, Puthezhath S. N, SMITH, Tenesha

    Published in Human genetics
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  3. 3
    Quantitative high-throughput measurement of gene expression with sub-zeptomole sensitivity by capillary electrophoresis

    Quantitative high-throughput measurement of gene expression with sub-zeptomole sensitivity by capillary electrophoresis by Spyres, Lea, Gaddis, Sally, Bedford, Ella, Arantes, Stacey, Liburd, Nikki, Powell, K. Leslie, Thames, Howard, Mitchell, David, Walborg, Earl, Rouabhia, Mahmoud, Aldaz, C. Marcelo, MacLeod, Michael C.

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