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2014 | 1 |
2015 | 1 |
2018 | 1 |
2024 | 0 |
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Clinical exome sequencing for genetic identification of rare Mendelian disorders.
JAMA. 2014 Nov 12;312(18):1880-7. doi: 10.1001/jama.2014.14604.
JAMA. 2014.
PMID: 25326637
Free PMC article.
Development of a molecular diagnostic test for Retinitis Pigmentosa in the Japanese population.
Maeda A, Yoshida A, Kawai K, Arai Y, Akiba R, Inaba A, Takagi S, Fujiki R, Hirami Y, Kurimoto Y, Ohara O, Takahashi M.
Maeda A, et al.
Jpn J Ophthalmol. 2018 Jul;62(4):451-457. doi: 10.1007/s10384-018-0601-x. Epub 2018 May 21.
Jpn J Ophthalmol. 2018.
PMID: 29785639
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Dependable and Efficient Clinical Molecular Diagnosis of Chinese RP Patient with Targeted Exon Sequencing.
Yang L, Cui H, Yin X, Dou H, Zhao L, Chen N, Zhang J, Zhang H, Li G, Ma Z.
Yang L, et al.
PLoS One. 2015 Oct 23;10(10):e0140684. doi: 10.1371/journal.pone.0140684. eCollection 2015.
PLoS One. 2015.
PMID: 26496393
Free PMC article.
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