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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1997 | 2 |
1999 | 1 |
2024 | 0 |
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Page 1
New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p.
Am J Med Genet. 1997 Sep 5;71(4):467-71.
Am J Med Genet. 1997.
PMID: 9286457
Nonsyndromic hearing impairment: unparalleled heterogeneity.
Van Camp G, Willems PJ, Smith RJ.
Van Camp G, et al.
Am J Hum Genet. 1997 Apr;60(4):758-64.
Am J Hum Genet. 1997.
PMID: 9106521
Free PMC article.
Review.
No abstract available.
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Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance.
Adato A, Kalinski H, Weil D, Chaib H, Korostishevsky M, Bonne-Tamir B.
Adato A, et al.
Am J Hum Genet. 1999 Jul;65(1):261-5. doi: 10.1086/302438.
Am J Hum Genet. 1999.
PMID: 10364543
Free PMC article.
No abstract available.
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