Citations (14)
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Read on this site (2)
Oana Vele & Iris Schrijver. (2008) Inherited hearing loss: molecular genetics and diagnostic testing. Expert Opinion on Medical Diagnostics 2:3, pages 231-248.
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Yu-Fen Guo, Yu-Fen Guo, Xiao-Wen Liu, Jing Guan, Ming-Kun Han, Da-Yong Wang, Ya-Li Zhao, Shao-Qi Rao & Qiu-ju Wang. (2008) GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects. Acta Oto-Laryngologica 128:3, pages 297-303.
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Articles from other publishers (12)
Betty Vohr & Susan Wiley. 2024. Avery's Diseases of the Newborn. Avery's Diseases of the Newborn
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Ning Yin, Jingjing Zhao, Panpan Zhang, Baofu Yu, Renjie Chai & Geng-Lin Li. (2023) Functional and developmental changes in the inner hair cell ribbon synapses caused by Myosin VI knockout and deafness-inducing point mutation. Cell Death Discovery 9:1.
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Tatiana Markova, Natalia Alekseeva, Maria Lalayants, Oxana Ryzhkova, Olga Shatokhina, Nailya Galeeva, Elena Bliznetz, Oleg Belov, Svetlana Chibisova, Alexander Polyakov & George Tavartkiladze. (2022) Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss. Journal of Personalized Medicine 12:11, pages 1843.
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Betty Vohr. 2018. Avery's Diseases of the Newborn. Avery's Diseases of the Newborn
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Andrew P. McGrath & Betty R. Vohr. (2017) Hearing Loss in the Newborn Infant: Early Hearing Detection and Intervention. NeoReviews 18:10, pages e587-e597.
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Hedyeh Javidnia, Nancy Carson, Michael Awubwa, Richard Byaruhanga, David Mack & Jean-Philippe Vaccani. (2014) Connexin gene mutations among ugandan patients with nonsyndromic sensorineural hearing loss. The Laryngoscope 124:9, pages E373-E376.
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Lynn M. Pique, Marie-Luise Brennan, Colin J. Davidson, Frederick Schaefer, John Greinwald Jr & Iris Schrijver. (2014)
Mutation analysis of the
SLC26A4
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FOXI1
and
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Bing Han, Liang Zong, Qian Li, Zhidong Zhang, Dayong Wang, Lan Lan, Jingxin Zhang, Yali Zhao & Qiuju Wang. (2013) Newborn genetic screening for high risk deafness-associated mutations with a new Tetra-primer ARMS PCR kit. International Journal of Pediatric Otorhinolaryngology 77:9, pages 1440-1445.
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Qiu–ju Wang, Rao Shao–qi, Guo Yu–fen, Li Qing–zhong, Zhao Hui, Zhao Li–dong, Yuan Hu, Zong Liang, Liu Qiong, Zhao Ya–li, Wang Da–yong, Han Ming–kun, Ji Yu–bin, Li Jian–qiang, Lan Lan, Yang Wei–yan, Shen Yan & Han Dong–yi. (2009) The genetic load for hereditary hearing impairment in Chinese population and its clinical implication. Journal of Otology 4:2, pages 98-105.
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Julie M. Schultz, Shaheen N. Khan, Zubair M. Ahmed, Saima Riazuddin, Ali M. Waryah, Dhananjay Chhatre, Matthew F. Starost, Barbara Ploplis, Stephanie Buckley, David Velásquez, Madhulika Kabra, Kwanghyuk Lee, Muhammad J. Hassan, Ghazanfar Ali, Muhammad Ansar, Manju Ghosh, Edward R. Wilcox, Wasim Ahmad, Glenn Merlino, Suzanne M. Leal, Sheikh Riazuddin, Thomas B. Friedman & Robert J. Morell. (2009) Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39. The American Journal of Human Genetics 85:1, pages 25-39.
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D. Bönsch, C.-M. Schmidt, P. Scheer, J. Bohlender, C. Neumann, A. am Zehnhoff-Dinnesen & T. Deufel. (2009) Ein neuer Genort für eine autosomal-dominante, nichtsyndromale Schwerhörigkeit (DFNA33) liegt auf Chromosom 13q34-qterA new gene locus for an autosomal-dominant non-syndromic hearing impairment (DFNA 33) is situated on chromosome 13q34-qter. HNO 57:4, pages 371-376.
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D. Bönsch, C.M. Schmidt, P. Scheer, J. Bohlender, C. Neumann, A. am Zehnhoff-Dinnesen & T. Deufel. (2008) Ein neuer Genort für eine autosomal dominante, nichtsyndromale Hörstörung (DFNA57) kartiert auf Chromosom 19p13.2 und überlappt mit DFNB15A new locus for an autosomal dominant, non-syndromic hearing impairment (DFNA57) located on chromosome 19p13.2 and overlapping with DFNB15. HNO 56:2, pages 177-182.
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