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1by Ahmed, Zubair M, Cindy Li, Xiaoyan, Powell, Shontell D, Riazuddin, Saima, Young, Terry-Lynn, Ramzan, Khushnooda, Ahmad, Zahoor, Luscombe, Sandra, Dhillon, Kiran, MacLaren, Linda, Ploplis, Barbara, Shotland, Lawrence I, Ives, Elizabeth, Riazuddin, Sheikh, Friedman, Thomas B, Morell, Robert J, Wilcox, Edward RGet access
Published in BMC Medical Genetics (2004)
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2by Ahmed, Zubair M, Cindy Li, Xiaoyan, Powell, Shontell D, Riazuddin, Saima, Young, Terry-Lynn, Ramzan, Khushnooda, Ahmad, Zahoor, Luscombe, Sandra, Dhillon, Kiran, MacLaren, Linda, Ploplis, Barbara, Shotland, Lawrence I, Ives, Elizabeth, Riazuddin, Sheikh, Friedman, Thomas B, Morell, Robert J, Wilcox, Edward RGet access
Published in BMC Medical Genetics (2004)
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3by Ahmed, Zubair M, Cindy Li, Xiaoyan, Powell, Shontell D, Riazuddin, Saima, Young, Terry-Lynn, Ramzan, Khushnooda, Ahmad, Zahoor, Luscombe, Sandra, Dhillon, Kiran, MacLaren, Linda, Ploplis, Barbara, Shotland, Lawrence I, Ives, Elizabeth, Riazuddin, Sheikh, Friedman, Thomas B, Morell, Robert J, Wilcox, Edward R“...Abstract Background Mutant alleles of TMPRSS3 are associated with nonsyndromic recessive deafness...”
Published 2004
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4by Ahmed, Zubair M., Cindy Li, Xiaoyan, Powell, Shontell D., Riazuddin, Saima, Young, Terry-Lynn, Ramzan, Khushnooda, Ahmad, Zahoor, Luscombe, Sandra, Dhillon, Kiran, MacLaren, Linda, Ploplis, Barbara, Shotland, Lawrence I., Ives, Elizabeth, Riazuddin, Seikh, Friedman, Thomas B., Morell, Robert J., Wilcox, Edward R.“...Background: Mutant alleles of TMPRSS3 are associated with nonsyndromic recessive deafness (DFNB8/B...”
Published 2004
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5by Doucette, Lance, Merner, Nancy D, Cooke, Sandra, Ives, Elizabeth, Galutira, Dante, Walsh, Vanessa, Walsh, Tom, MacLaren, Linda, Cater, Tracey, Fernandez, Bridget, Green, Jane S, Wilcox, Edward R, Shotland, Larry, Li, X C, Lee, Ming, King, Mary-Claire, Young, Terry-Lynn“... the deafness trait to 10q21-22 (max LOD score of 4.0; D10S196) and fine mapping revealed a 16 Mb ancestral...”
Published in European Journal of Human Genetics (2009)
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6by Young, Terry-Lynn, Ives, Elizabeth, Lynch, Eric, Person, Richard, Snook, Stephanie, MacLaren, Linda, Cator, Tracey, Griffin, Anne, Fernandez, Bridget, Lee, Ming K., King, Mary-Claire“.... Dominant deafness defined by DFNA38 is more severe than deafness of Wolfram syndrome patients and lacks any...”
Published in Human Molecular Genetics (2001)
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7by Abdelfatah, Nelly, McComiskey, David A, Doucette, Lance, Griffin, Anne, Moore, Susan J, Negrijn, Carol, Hodgkinson, Kathy A, King, Justin J, Larijani, Mani, Houston, Jim, Stanton, Susan G, Young, Terry-Lynn“... to disrupt multimerization of KCNQ4 subunits. Surprisingly, 10/23 deaf relatives are non-carriers of p.S269...”
Published in European Journal of Human Genetics (2013)
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8by Pater, Justin A., Benteau, Tammy, Griffin, Anne, Penney, Cindy, Stanton, Susan G., Predham, Sarah, Kielley, Bernadine, Squires, Jessica, Zhou, Jiayi, Li, Quan, Abdelfatah, Nelly, O’Rielly, Darren D., Young, Terry-Lynn“... sequencing of probands for deafness alleles (n = 23) that we previously identified in this founder population...”
Published in Human Genetics (2016)
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9by Pater, Justin A., Penney, Cindy, O’Rielly, Darren D., Griffin, Anne, Kamal, Lara, Brownstein, Zippora, Vona, Barbara, Vinkler, Chana, Shohat, Mordechai, Barel, Ortal, Young, Terry-Lynn“..., discovery of dominant genes including deafness genes (DFNA) remains challenging. We report a new DFNA gene...”
Published in Human Genetics (2022)
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