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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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2014 | 1 |
2015 | 2 |
2022 | 1 |
2024 | 0 |
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Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy.
Heart. 2015 Feb;101(4):294-301. doi: 10.1136/heartjnl-2014-306387. Epub 2014 Oct 28.
Heart. 2015.
PMID: 25351510
Free PMC article.
Application of targeted multi-gene panel testing for the diagnosis of inherited peripheral neuropathy provides a high diagnostic yield with unexpected phenotype-genotype variability.
Antoniadi T, Buxton C, Dennis G, Forrester N, Smith D, Lunt P, Burton-Jones S.
Antoniadi T, et al.
BMC Med Genet. 2015 Sep 21;16:84. doi: 10.1186/s12881-015-0224-8.
BMC Med Genet. 2015.
PMID: 26392352
Free PMC article.
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Congenital muscle dystrophies: Role of singleton whole exome sequencing in countries with limited resources.
Masri AT, Oweis L, Qudah AA, El-Shanti H.
Masri AT, et al.
Clin Neurol Neurosurg. 2022 Jun;217:107271. doi: 10.1016/j.clineuro.2022.107271. Epub 2022 May 2.
Clin Neurol Neurosurg. 2022.
PMID: 35533453
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