Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29
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 (12.01.2001)
Published in Cell (12.01.2001)
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Dominant modifier DFNM1 suppresses recessive deafness DFNB26
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
Published in Nature genetics (01.12.2000)
Published in Nature genetics (01.12.2000)
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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
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 (01.11.2001)
Published in Human genetics (01.11.2001)
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Quantitative high-throughput measurement of gene expression with sub-zeptomole sensitivity by capillary electrophoresis
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.
Published in Analytical biochemistry (15.10.2005)
Published in Analytical biochemistry (15.10.2005)
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