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Year | Number of Results |
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2002 | 1 |
2004 | 1 |
2007 | 1 |
2024 | 0 |
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Effectiveness of sequencing connexin 26 (GJB2) in cases of familial or sporadic childhood deafness referred for molecular diagnostic testing.
Genet Med. 2002 Jul-Aug;4(4):279-88. doi: 10.1097/00125817-200207000-00006.
Genet Med. 2002.
PMID: 12172394
Free article.
Spectrum and frequencies of mutations in the GJB2 (Cx26) gene among 156 Czech patients with pre-lingual deafness.
Seeman P, Malíková M, Rasková D, Bendová O, Groh D, Kubálková M, Sakmaryová I, Seemanová E, Kabelka Z.
Seeman P, et al.
Clin Genet. 2004 Aug;66(2):152-7. doi: 10.1111/j.1399-0004.2004.00283.x.
Clin Genet. 2004.
PMID: 15253766
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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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