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For: Wou K, Chung WK, Wapner RJ. Laboratory considerations for prenatal genetic testing. Semin Perinatol 2018;42:307-13. [PMID: 30206017 DOI: 10.1053/j.semperi.2018.07.020] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
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1 Wain KE, Azzariti DR, Goldstein JL, Johnson AK, Krautscheid P, Lepore B, O'Daniel JM, Ritter D, Savatt JM, Riggs ER, Martin CL. Variant interpretation is a component of clinical practice among genetic counselors in multiple specialties. Genet Med 2020;22:785-92. [PMID: 31754268 DOI: 10.1038/s41436-019-0705-9] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
2 Gentile M, Fanelli T, Lepri FR, Gentile A, Orsini P, Volpe P, Novelli A, Ficarella R. First prenatal case of Noonan syndrome with SOS2 mutation: Implications of early diagnosis for genetic counseling. Am J Med Genet A 2021;185:1897-902. [PMID: 33750022 DOI: 10.1002/ajmg.a.62180] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Krstić N, Običan SG. Current landscape of prenatal genetic screening and testing. Birth Defects Res 2020;112:321-31. [PMID: 31633301 DOI: 10.1002/bdr2.1598] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 1.3] [Reference Citation Analysis]