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Sequencing as a first-line methodology for cystic fibrosis carrier screening.
Genet Med. 2019 Nov;21(11):2569-2576. doi: 10.1038/s41436-019-0525-y. Epub 2019 Apr 30.
Genet Med. 2019.
PMID: 31036917
Free PMC article.
Correction: Sequencing as a first-line methodology for cystic fibrosis carrier screening.
Beauchamp KA, Taber KAJ, Grauman PV, Spurka L, Lim-Harashima J, Svenson A, Goldberg JD, Muzzey D.
Beauchamp KA, et al. Among authors: lim harashima j.
Genet Med. 2019 Oct;21(10):2407-2408. doi: 10.1038/s41436-019-0543-9.
Genet Med. 2019.
PMID: 31089271
Free PMC article.
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Fragile X syndrome carrier screening accompanied by genetic consultation has clinical utility in populations beyond those recommended by guidelines.
Johansen Taber K, Lim-Harashima J, Naemi H, Goldberg J.
Johansen Taber K, et al. Among authors: lim harashima j.
Mol Genet Genomic Med. 2019 Dec;7(12):e1024. doi: 10.1002/mgg3.1024. Epub 2019 Nov 6.
Mol Genet Genomic Med. 2019.
PMID: 31694075
Free PMC article.
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Perceived clinical utility of a test for predicting inadequate response to TNF inhibitor therapies in rheumatoid arthritis: results from a decision impact study.
Pappas DA, Brittle C, Mossell JE 3rd, Withers JB, Lim-Harashima J, Kremer JM.
Pappas DA, et al. Among authors: lim harashima j.
Rheumatol Int. 2021 Mar;41(3):585-593. doi: 10.1007/s00296-020-04746-7. Epub 2020 Nov 30.
Rheumatol Int. 2021.
PMID: 33258003
Free PMC article.
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