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	1.	Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans. [electronic resource] by Dias, Alex Marcel Moreira Lezirovitz, Karina Nicastro, Fernanda Stávale Mendes, Beatriz C A Mingroni-Netto, Regina Célia Producer: 20190410 In: Journal of human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Is autosomal recessive deafness associated with oculocutaneous albinism a "coincidence syndrome"? [electronic resource] by Lezirovitz, Karina Nicastro, Fernanda Stávale Pardono, Eliete Abreu-Silva, Ronaldo Serafim Batissoco, Ana Carla Neustein, Isaac Spinelli, Mauro Mingroni-Netto, Regina Célia Producer: 20061006 In: Journal of human genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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