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A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects.
Beck DB, Cho MT, Millan F, Yates C, Hannibal M, O'Connor B, Shinawi M, Connolly AM, Waggoner D, Halbach S, Angle B, Sanders V, Shen Y, Retterer K, Begtrup A, Bai R, Chung WK. Beck DB, et al. Among authors: yates c. Neurogenetics. 2016 Jul;17(3):173-8. doi: 10.1007/s10048-016-0482-4. Epub 2016 Apr 19. Neurogenetics. 2016. PMID: 27094857
Adopted individuals' interest in elective genomic testing.
Edgar J, Bao A, Maga T, Schwartz M, Yates C, Spencer S. Edgar J, et al. Among authors: yates c. J Med Genet. 2022 Feb;59(2):197-203. doi: 10.1136/jmedgenet-2020-107503. Epub 2020 Dec 21. J Med Genet. 2022. PMID: 33443090
Skeletal fluorosis secondary to methoxyflurane use for chronic pain.
Park YA, Plehwe WE, Varatharajah K, Hale S, Christie M, Yates CJ. Park YA, et al. Among authors: yates cj. JBMR Plus. 2024 Mar 7;8(5):ziae032. doi: 10.1093/jbmrpl/ziae032. eCollection 2024 May. JBMR Plus. 2024. PMID: 38577522 Free PMC article.
787 results