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| Fecha de publicación | Título | Autor(es) | | ene-2023 | A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29 | Modamio-Høybjør, S; Moreno-Pelayo, MA; Mencía, A; del Castillo, I; Chardenoux, S; Armenta, D; Lathrop, M; Petite, C; Moreno, F |
| 26-ene-2026 | A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28–29 | Modamio-Høybjør, S; Moreno-Pelayo, MA; Mencía, A; del Castillo, I; Chardenoux, S; Armenta, D; Lathrop, M; Petit, C; Moreno, F |
| feb-2004 | A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci | Modamio-Høybjør, S; Moreno-Pelayo, MA; Mencía, A; del Castillo, I; Chardenoux, S; Morais, D; Lathrop, M; Petite, C; Moreno, F |
| nov-2023 | DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23 | Moreno-Pelayo, MA; Modamio-Høybjør, S; Mencía, A; del Castillo, I; Chardenoux, S; Fernández-Burriel, M; Lathrop, M; Petite, C; Moreno, F |
| jul-2011 | DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss | Hildebrand, MS; Morín, M; Meyer, NC; Mayo-Merino, F; Modamio-Høybjør, S; Mencía, A; Olavarrieta, L; Morales-Angulo, Carmelo; Nishimura, CJ; Workman, H; DeLuca, AP; del Castillo, I; Taylor, KR; Tompkins, B; Goodman, CW; Schrauwen, I; Van Wesemael, M; Lachlan, K; Shearer, AE; Braun, TA; Huygen, PLM; Kremer, H; Van Camp, G; Moreno, F; Casavant, TL; Smith, RJH; Moreno-Pelayo, MA |
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