| scholarly article | Q13442814 |
| P2093 | author name string | Wayne S | |
| Smith RJ | |||
| Chen A | |||
| Fukushima K | |||
| Sheffield VC | |||
| Ni L | |||
| Van Camp G | |||
| O'Neill ME | |||
| Nishimura D | |||
| Wilcox ER | |||
| Marietta J | |||
| Negrini C | |||
| Van Laer L | |||
| P433 | issue | 6 | |
| P921 | main subject | hearing loss | Q16035842 |
| P304 | page(s) | 853-856 | |
| P577 | publication date | 1996-06-01 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6. | |
| P478 | volume | 5 |
| Q50490256 | A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13. |
| Q30501418 | A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3. |
| Q35663740 | A novel EYA4 mutation causing hearing loss in a Chinese DFNA family and genotype-phenotype review of EYA4 in deafness |
| Q38084832 | Atypical protein phosphatases: emerging players in cellular signaling |
| Q33639128 | Beginning of a molecular era in hearing and deafness |
| Q33834697 | Biology of chromosome 6. |
| Q28585781 | Eya4-deficient mice are a model for heritable otitis media |
| Q41244075 | Genes responsible for human hereditary deafness: symphony of a thousand |
| Q41103360 | Genetics of deafness |
| Q48542052 | Hearing loss in the laminin-deficient dy mouse model of congenital muscular dystrophy |
| Q35550640 | Human Nonsyndromic Sensorineural Deafness |
| Q34407010 | Human sequences homologous to the gene for the cochlear protein Ocp-II do not map to currently known non-syndromic hearing loss loci |
| Q34426824 | Identification of I411K, a novel missense EYA4 mutation causing autosomal dominant non‑syndromic hearing loss |
| Q50489817 | Is there a relationship between U-shaped audiograms and mutations in connexin 26? |
| Q33965187 | Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes |
| Q34747004 | Non-syndromic autosomal-dominant deafness |
| Q41364778 | Non-syndromic dominant sensorineural hearing loss: from a few phenotypes to many genotypes |
| Q24680416 | Nonsyndromic hearing impairment: unparalleled heterogeneity |
| Q71917074 | Sensorineural hearing loss in children |
| Q50490264 | The DFNA10 phenotype. |
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