Citations (21)
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Articles from other publishers (11)
Per Wändell, Xinjun Li, Axel C. Carlsson, Jan Sundquist & Kristina Sundquist. (2021) Hearing impairment among children in Sweden with foreign‐born parents and natives: A national Swedish study. Acta Paediatrica 110:10, pages 2817-2824.
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Charlotte Stübner, Traci Flynn, Christopher Gillberg, Elisabeth Fernell & Carmela Miniscalco. (2019) Schoolchildren with unilateral or mild to moderate bilateral sensorineural hearing loss should be screened for neurodevelopmental problems. Acta Paediatrica 109:7, pages 1430-1438.
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K. Sigvard Olsson, Olof Wålinder, Ulf Jansson, Maria Wilbe, Marie-Louise Bondeson, Eva-Lena Stattin, Ruma Raha-Chowdhury & Roger Williams. (2017) Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes. Hereditas 154:1.
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Der-Chung Lai, Yen-Cheng Tseng, Cheng-Yu Lin & How-Ran Guo. (2014) Screening, rubella vaccination, and childhood hearing impairment in Taiwan. Research in Developmental Disabilities 35:11, pages 3182-3190.
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Marie-Louise Barrenäs, Åsa Bratthall & Jovanna Dahlgren. (2005) The association between short stature and sensorineural hearing loss. Hearing Research 205:1-2, pages 123-130.
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Eero Vartiainen, Piia Kemppinen & Seppo Karjalainen. (1997) Prevalence and etiology of bilateral sensorineural hearing impairment in a Finnish childhood population. International Journal of Pediatric Otorhinolaryngology 41:2, pages 175-185.
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