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	1.	A novel M163L mutation in connexin 26 causing cell death and associated with autosomal dominant hearing loss. [electronic resource] by Matos, T D Caria, H Simões-Teixeira, H Aasen, T Dias, O Andrea, M Kelsell, D P Fialho, G Producer: 20080829 In: Hearing research vol. 240 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A novel hearing-loss-related mutation occurring in the GJB2 basal promoter. [electronic resource] by Matos, T D Caria, H Simões-Teixeira, H Aasen, T Nickel, R Jagger, D J O'Neill, A Kelsell, D P Fialho, G Producer: 20071129 In: Journal of medical genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	WFS1 and non-syndromic low-frequency sensorineural hearing loss: a novel mutation in a Portuguese case. [electronic resource] by Gonçalves, A C Matos, T D Simões-Teixeira, H R Pimenta Machado, M Simão, M Dias, O P Andrea, M Fialho, G Caria, H Producer: 20140414 In: Gene vol. 538 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Assessing Noncoding Sequence Variants of GJB2 for Hearing Loss Association. [electronic resource] by Matos, T D Simões-Teixeira, H Caria, H Cascão, R Rosa, H O'Neill, A Dias, O Andrea, M E Kelsell, D P Fialho, G Producer: 20120823 In: Genetics research international vol. 2011 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)