Cited by

• Auditory and speech outcomes of cochlear implantation in patients with Waardenburg syndrome: a meta-analysis.

  Qin F, Guo S, Yin X, Lu X, Ma J. Qin F, et al. Front Neurol. 2024 Jul 11;15:1372736. doi: 10.3389/fneur.2024.1372736. eCollection 2024. Front Neurol. 2024. PMID: 39055322 Free PMC article.
• CRISPR/Cas9-mediated correction of MITF homozygous point mutation in a Waardenburg syndrome 2A pig model.

  Yao J, Wang Y, Cao C, Song R, Bi D, Zhang H, Li Y, Qin G, Hou N, Zhang N, Zhang J, Guo W, Yang S, Wang Y, Zhao J. Yao J, et al. Mol Ther Nucleic Acids. 2021 Apr 16;24:986-999. doi: 10.1016/j.omtn.2021.04.009. eCollection 2021 Jun 4. Mol Ther Nucleic Acids. 2021. PMID: 34094716 Free PMC article.
• [Anatomical and pathological aspects of the electrical stimulation of the deaf inner ear (author's transl)].

  Spoendlin H. Spoendlin H. Arch Otorhinolaryngol. 1979;223(1):1-75. doi: 10.1007/BF00455076. Arch Otorhinolaryngol. 1979. PMID: 383058 Review. German. No abstract available.
• Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4.

  Bondurand N, Dastot-Le Moal F, Stanchina L, Collot N, Baral V, Marlin S, Attie-Bitach T, Giurgea I, Skopinski L, Reardon W, Toutain A, Sarda P, Echaieb A, Lackmy-Port-Lis M, Touraine R, Amiel J, Goossens M, Pingault V. Bondurand N, et al. Am J Hum Genet. 2007 Dec;81(6):1169-85. doi: 10.1086/522090. Epub 2007 Oct 22. Am J Hum Genet. 2007. PMID: 17999358 Free PMC article.
• New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing.

  Li W, Mei L, Chen H, Cai X, Liu Y, Men M, Liu XZ, Yan D, Ling J, Feng Y. Li W, et al. Neural Plast. 2019 Feb 27;2019:7143458. doi: 10.1155/2019/7143458. eCollection 2019. Neural Plast. 2019. PMID: 30936914 Free PMC article.