All papers authored by Hela Azaiez
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2021
Barbara Vona 
,
Neda Mazaheri ,
Sheng-Jia Lin ,
Lucy A. Dunbar ,
Reza Maroofian,
Hela Azaiez ,
Kevin T. Booth ,
Sandrine Vitry ,
Aboulfazl Rad ,
Franz Rüschendorf ,
Pratishtha Varshney ,
Ben Fowler,
Christian Beetz ,
Kumar N. Alagramam,
David Murphy
and 11 other authors
,
Neda Mazaheri ,
Sheng-Jia Lin ,
Lucy A. Dunbar ,
Reza Maroofian,
Hela Azaiez ,
Kevin T. Booth ,
Sandrine Vitry ,
Aboulfazl Rad ,
Franz Rüschendorf ,
Pratishtha Varshney ,
Ben Fowler,
Christian Beetz ,
Kumar N. Alagramam,
David Murphy
and 11 other authors
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans
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Yoel Hirsch,
Chayada Tangshewinsirikul,
Kevin T. Booth ,
Hela Azaiez ,
Devorah Yefet,
Adina Quint,
Tzvi Weiden,
Zippora Brownstein,
Michal Macarov,
Bella Davidov,
John Pappas ,
Rachel Rabin,
Margaret A. Kenna,
Andrea M. Oza,
Katherine Lafferty
and 13 other authors
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,
Hela Azaiez ,
Devorah Yefet,
Adina Quint,
Tzvi Weiden,
Zippora Brownstein,
Michal Macarov,
Bella Davidov,
John Pappas ,
Rachel Rabin,
Margaret A. Kenna,
Andrea M. Oza,
Katherine Lafferty
and 13 other authors
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2020
Kevin T. Booth,
Amama Ghaffar,
Muhammad Rashid,
Luke T. Hovey,
Mureed Hussain,
Kathy Frees,
Erika M. Renkes,
Carla J. Nishimura,
Mohsin Shahzad,
Richard J. Smith,
Zubair Ahmed,
Hela Azaiez ,
Saima Riazuddin
,
Saima Riazuddin
Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing loss
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Kevin T. Booth ,
Hela Azaiez ,
Richard J. H. Smith
,
Hela Azaiez ,
Richard J. H. Smith
DFNA5 (GSDME) c.991-15_991-13delTTC: Founder Mutation or Mutational Hotspot?
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