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

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Dominant modifier DFNM1 suppresses recessive deafness DFNB26 von Wilcox, Edward R, Riazuddin, Saima, Castelein, Caley M, Ahmed, Zubair M, Lalwani, Anil K, Mastroianni, Mary A, Naz, Sadaf, Smith, Tenesha N, Liburd, Nikki A, Friedman, Thomas B, Griffith, Andrew J, Riazuddin, Sheikh

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

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Quantitative high-throughput measurement of gene expression with sub-zeptomole sensitivity by capillary electrophoresis von 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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