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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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2002 | 1 |
2003 | 1 |
2007 | 1 |
2024 | 0 |
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Genotypic and phenotypic correlations of DFNB1-related hearing impairment in the Midwestern United States.
Arch Otolaryngol Head Neck Surg. 2003 Aug;129(8):836-40. doi: 10.1001/archotol.129.8.836.
Arch Otolaryngol Head Neck Surg. 2003.
PMID: 12925341
Effectiveness of sequencing connexin 26 (GJB2) in cases of familial or sporadic childhood deafness referred for molecular diagnostic testing.
Wu BL, Lindeman N, Lip V, Adams A, Amato RS, Cox G, Irons M, Kenna M, Korf B, Raisen J, Platt O.
Wu BL, et al.
Genet Med. 2002 Jul-Aug;4(4):279-88. doi: 10.1097/00125817-200207000-00006.
Genet Med. 2002.
PMID: 12172394
Free article.
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Compound heterozygosity for dominant and recessive GJB2 mutations: effect on phenotype and review of the literature.
Welch KO, Marin RS, Pandya A, Arnos KS.
Welch KO, et al.
Am J Med Genet A. 2007 Jul 15;143A(14):1567-73. doi: 10.1002/ajmg.a.31701.
Am J Med Genet A. 2007.
PMID: 17431919
Review.
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