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JARID2 haploinsufficiency is associated with a clinically distinct neurodevelopmental syndrome.
Genet Med. 2021 Feb;23(2):374-383. doi: 10.1038/s41436-020-00992-z. Epub 2020 Oct 20.
Genet Med. 2021.
PMID: 33077894
Free article.
FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?
Myers A, du Souich C, Yang CL, Borovik L, Mwenifumbo J, Rupps R, Study C, Lehman A, Boerkoel CF.
Myers A, et al. Among authors: study c.
Am J Med Genet A. 2017 Dec;173(12):3172-3181. doi: 10.1002/ajmg.a.38462. Epub 2017 Sep 8.
Am J Med Genet A. 2017.
PMID: 28884888
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Shortened consent forms for genome-wide sequencing: Parent and provider perspectives.
Hitchcock EC, Study C, Elliott AM.
Hitchcock EC, et al. Among authors: study c.
Mol Genet Genomic Med. 2020 Jul;8(7):e1254. doi: 10.1002/mgg3.1254. Epub 2020 May 8.
Mol Genet Genomic Med. 2020.
PMID: 32383361
Free PMC article.
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Associations of hypomagnesemia in patients seeking a first treatment of alcohol use disorder.
Hernández-Rubio A, Sanvisens A, Barbier-Torres L, Blanes R, Miquel L, Torrens M, Rubio G, Bolao F, Zuluaga P, Fuster D, Rodríguez de Fonseca F, Farré M, Muga R; CohRTA.
Hernández-Rubio A, et al.
Drug Alcohol Depend. 2023 Apr 1;245:109822. doi: 10.1016/j.drugalcdep.2023.109822. Epub 2023 Feb 24.
Drug Alcohol Depend. 2023.
PMID: 36893509
Free article.
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