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- [43] The autosomal recessive non-syndromic deafness loci, DFNB8 and DFNB10 on human chromosome 21q22.3, are distinct loci CYTOGENETICS AND CELL GENETICS, 1999, 86 (01): : 19 - 19
- [45] Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53 Molecular Genetics and Genomics, 2015, 290 : 1327 - 1334
- [46] A new autosomal recessive nonsyndromic hearing impairment locus DFNB96 on chromosome 1p36.31–p36.13 Journal of Human Genetics, 2011, 56 : 866 - 868
- [47] DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2 Human Genetics, 2011, 129 : 379 - 385