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Novel frameshift mutation in LIS1 gene is a probable cause of lissencephaly: a case report.
BMC Pediatr. 2022 Sep 14;22(1):545. doi: 10.1186/s12887-022-03595-6.
BMC Pediatr. 2022.
PMID: 36100855
Free PMC article.
[Bilateral paramedian thalamic infraction due artery of Percheron occlusion].
Baltar Yanes F, Turcatti E, González Rabelino G.
Baltar Yanes F, et al.
Andes Pediatr. 2021 Dec;92(6):924-929. doi: 10.32641/andespediatr.v92i6.3595. Epub 2021 Sep 8.
Andes Pediatr. 2021.
PMID: 35506805
Free article.
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