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recseg k
(3 results)?
Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants.
Genet Med. 2022 Jan;24(1):130-145. doi: 10.1016/j.gim.2021.09.001. Epub 2021 Nov 30.
Genet Med. 2022.
PMID: 34906502
Free article.
Evaluating the model of offering expanded genetic carrier screening to high school students within the Sydney Jewish community.
Barlow-Stewart K, Bardsley K, Elan E, Fleming J, Berman Y, Fleischer R, Recsei K, Goldberg D, Tucker J, Burnett L.
Barlow-Stewart K, et al. Among authors: recsei k.
J Community Genet. 2022 Feb;13(1):121-131. doi: 10.1007/s12687-021-00567-8. Epub 2021 Nov 30.
J Community Genet. 2022.
PMID: 34846685
Free PMC article.
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