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- W2029851250 abstract "The use of molecular techniques in respect of the rare X-linked non-syndromic form of genetic deafness demonstrates that this is a genetically heterogeneous disorder, with evidence for at least two separate gene loci on the X chromosome. Audiological heterogencity in this condition is emphasized by the observation of both mixed deafness and sensorincural deafness in pedigrees showing evidence for linkage to Xq13-q21. The importance and shortcomings of the audiogram in assessing females who are known gene carriers is discussed." @default.
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- W2029851250 title "Clinical and genetic heterogeneity in X-linked deafness" @default.
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- W2029851250 doi "https://doi.org/10.3109/03005369209077878" @default.
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