X.Z. Liu

Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss

X.Z. Liu · Human Molecular Genetics · 2000 · 185 citations

Life Sciences, Genetics, Molecular Genetics +15

Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness

X.Z. Liu · Human Molecular Genetics · 2001 · 140 citations

Life Sciences, Genetics, Molecular Genetics +16

Relation between choice of partner and high frequency of connexin-26 deafness

Walter E. Nance, X.Z. Liu, Arti Pandya · The Lancet · 2000 · 73 citations

Life Sciences, Communication, Genetics +4

Audiological and genetic features of the<i>mt</i>DNA mutations

X.Z. Liu, Simón I. Angeli, Xiao Mei Ouyang et al. · Acta Oto-Laryngologica · 2008 · 30 citations

Life Sciences, Genetics, Molecular Genetics +17

The Clinical Presentation of DFNB2

X.Z. Liu · Advances in oto-rhino-laryngology · 2002 · 10 citations

Medicine, Pathology, Molecular Pathology +1