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Xq22 deletions and correlation with distinct neurological disease traits in females: Further evidence for a contiguous gene syndrome.
Hum Mutat. 2020 Jan;41(1):150-168. doi: 10.1002/humu.23902. Epub 2019 Nov 14.
Hum Mutat. 2020.
PMID: 31448840
Free PMC article.
Hearing loss in children with mitochondrial disorders.
Chennupati SK, Levi J, Loftus P, Jornlin C, Morlet T, O'Reilly RC.
Chennupati SK, et al. Among authors: jornlin c.
Int J Pediatr Otorhinolaryngol. 2011 Dec;75(12):1519-24. doi: 10.1016/j.ijporl.2011.08.019. Epub 2011 Oct 5.
Int J Pediatr Otorhinolaryngol. 2011.
PMID: 21982076
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