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Year | Number of Results |
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1995 | 2 |
1996 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 331485
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Genes responsible for human hereditary deafness: symphony of a thousand.
Nat Genet. 1996 Dec;14(4):385-91. doi: 10.1038/ng1296-385.
Nat Genet. 1996.
PMID: 8944017
Review.
Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q.
Fukushima K, Ramesh A, Srisailapathy CR, Ni L, Chen A, O'Neill M, Van Camp G, Coucke P, Smith SD, Kenyon JB, et al.
Fukushima K, et al.
Hum Mol Genet. 1995 Sep;4(9):1643-8. doi: 10.1093/hmg/4.9.1643.
Hum Mol Genet. 1995.
PMID: 8541854
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Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population.
Baldwin CT, Weiss S, Farrer LA, De Stefano AL, Adair R, Franklyn B, Kidd KK, Korostishevsky M, Bonné-Tamir B.
Baldwin CT, et al.
Hum Mol Genet. 1995 Sep;4(9):1637-42. doi: 10.1093/hmg/4.9.1637.
Hum Mol Genet. 1995.
PMID: 8541853
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