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Results: 3

Authors: Yasunaga, S Grati, M Cohen-Salmon, M El-Amraoui, A Mustapha, M Salem, N El-Zir, E Loiselet, J Petit, C
Citation: S. Yasunaga et al., A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness, NAT GENET, 21(4), 1999, pp. 363-369

Authors: Mustapha, M Weil, D Chardenoux, S Elias, S El-Zir, E Beckmann, JS Loiselet, J Petit, C
Citation: M. Mustapha et al., An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21, HUM MOL GEN, 8(3), 1999, pp. 409-412

Authors: Mustapha, M Salem, N Weil, D El-Zir, E Loiselet, J Petit, C
Citation: M. Mustapha et al., Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness, EUR J HUM G, 6(6), 1998, pp. 548-551
Risultati: 1-3 |