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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1994 1
1996 1
2000 1
2004 1
2007 1
2008 1
2010 1
2011 1
2013 2
2014 4
2015 2
2019 1
2020 2
2021 4
2022 3
2024 0

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PubMed for id: 318614

23 results

Results by year

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Page 1
Benefits of Exome Sequencing in Children with Suspected Isolated Hearing Loss.
Van Heurck R, Carminho-Rodrigues MT, Ranza E, Stafuzza C, Quteineh L, Gehrig C, Hammar E, Guipponi M, Abramowicz M, Senn P, Guinand N, Cao-Van H, Paoloni-Giacobino A. Van Heurck R, et al. Genes (Basel). 2021 Aug 20;12(8):1277. doi: 10.3390/genes12081277. Genes (Basel). 2021. PMID: 34440452 Free PMC article.
Novel KCNQ4 variants in different functional domains confer genotype- and mechanism-based therapeutics in patients with nonsyndromic hearing loss.
Lee SY, Choi HB, Park M, Choi IS, An J, Kim A, Kim E, Kim N, Han JH, Kim MY, Lee SM, Oh DY, Kim BJ, Yi N, Kim NKD, Lee C, Park WY, Koh YI, Gee HY, Cho HS, Kang TM, Choi BY. Lee SY, et al. Exp Mol Med. 2021 Jul;53(7):1192-1204. doi: 10.1038/s12276-021-00653-4. Epub 2021 Jul 28. Exp Mol Med. 2021. PMID: 34316018 Free PMC article.
23 results