R01 DC02942-02/DC/NIDCD NIH HHS/United States[Grants and Funding] - Search Results

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Subject: R01 DC02942-02/DC/NIDCD NIH HHS/United States[Gra - PubMed

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Year	Number of Results
1998	1
1999	2
2024	0

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Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss.

Kelley PM, Harris DJ, Comer BC, Askew JW, Fowler T, Smith SD, Kimberling WJ. Kelley PM, et al. Am J Hum Genet. 1998 Apr;62(4):792-9. doi: 10.1086/301807. Am J Hum Genet. 1998. PMID: 9529365 Free PMC article.

Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1).

Cohn ES, Kelley PM, Fowler TW, Gorga MP, Lefkowitz DM, Kuehn HJ, Schaefer GB, Gobar LS, Hahn FJ, Harris DJ, Kimberling WJ. Cohn ES, et al. Pediatrics. 1999 Mar;103(3):546-50. doi: 10.1542/peds.103.3.546. Pediatrics. 1999. PMID: 10049954

Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss.

Talebizadeh Z, Kelley PM, Askew JW, Beisel KW, Smith SD. Talebizadeh Z, et al. Hum Mutat. 1999;14(6):493-501. doi: 10.1002/(SICI)1098-1004(199912)14:6<493::AID-HUMU8>3.0.CO;2-P. Hum Mutat. 1999. PMID: 10571947

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