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Expanding the phenotypic spectrum of ARCN1-related syndrome.
Genet Med. 2022 Jun;24(6):1227-1237. doi: 10.1016/j.gim.2022.02.005. Epub 2022 Mar 14.
Genet Med. 2022.
PMID: 35300924
Free PMC article.
Rapid implementation of telegenetic services during the COVID-19 pandemic allowed continuing patient access, but not equally for all.
Noss R, Carlotti K, Leingang D, Flannery D.
Noss R, et al. Among authors: carlotti k.
Health Technol (Berl). 2022;12(4):839-844. doi: 10.1007/s12553-022-00670-x. Epub 2022 Apr 18.
Health Technol (Berl). 2022.
PMID: 35464100
Free PMC article.
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Perceived barriers to paternal expanded carrier screening following a positive maternal result: To screen or not to screen.
Carlotti K, Hines K, Weida J, Lah M, Schwantes-An TH.
Carlotti K, et al.
J Genet Couns. 2021 Apr;30(2):470-477. doi: 10.1002/jgc4.1333. Epub 2020 Oct 3.
J Genet Couns. 2021.
PMID: 33010192
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