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Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform

• Authors : De Keulenaer, Sarah; Hellemans, Jan; Lefever, Steve

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Genetic testing for hearing impairment.

• Authors : Topsakal V; Departement of Otorhinolaryngology, University Hospital Antwerp, UA, Belgium. ; Van Camp G

Subjects: Genetic Testing*; Hearing Loss/Hearing Loss/Hearing Loss/*genetics; Belgium

• Source: B-ENT [B-ENT] 2005; Vol. 1 (3), pp. 125-35.Publisher: Royal Belgian Society for Ear, Nose, Throat, Head and Neck surgery Country of Publication: Belgium NLM ID: 101247842

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Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method.

• Authors : Storm K; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.; Willocx S

Subjects: Connexins/Connexins/Connexins/*genetics ; Genetic Carrier Screening/Genetic Carrier Screening/Genetic Carrier Screening/*methods ; Genetic Testing/Genetic Testing/Genetic Testing/*methods

• Source: Human mutation [Hum Mutat] 1999; Vol. 14 (3), pp. 263-6.Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print Cited Medium: Print ISSN: 1059-7794 (Print)

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The fate and future of patents on human genes and genetic diagnostic methods

• Authors : Huys, Isabelle; Matthijs, Gert; Van Overwalle, Geertrui

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