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Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.
Funct Integr Genomics. 2022 Jun;22(3):291-315. doi: 10.1007/s10142-021-00819-3. Epub 2022 Jan 31.
Funct Integr Genomics. 2022.
PMID: 35098403
NDE1-related disorders: A recurrent NDE1 pathogenic variant causing Lissencephaly 4 can also be associated with microhydranencephaly.
Bas H, Saylisoy S, Cilingir O, Gokalp EE, Kocagil S, Yarar C, Aras BD, Artan S.
Bas H, et al. Among authors: gokalp ee.
Am J Med Genet A. 2022 Jan;188(1):326-331. doi: 10.1002/ajmg.a.62508. Epub 2021 Sep 25.
Am J Med Genet A. 2022.
PMID: 34562061
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A pediatric BAL case with double Ph chromosomes and trisomy 5.
Gunden G, Isik S, Ozdemir C, Cİlİngİr O, Bor O, Gokalp EE, Kocagil S, Artan S, Aras BD.
Gunden G, et al. Among authors: gokalp ee.
Cancer Genet. 2021 Nov;258-259:7-9. doi: 10.1016/j.cancergen.2021.06.005. Epub 2021 Jun 22.
Cancer Genet. 2021.
PMID: 34225100
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A novel SACS p.Pro4154GlnfsTer20 mutation in a family with autosomal recessive spastic ataxia of Charlevoix-Saguenay.
Samanci B, Gokalp EE, Bilgic B, Gurvit H, Artan S, Hanagasi HA.
Samanci B, et al. Among authors: gokalp ee.
Neurol Sci. 2021 Jul;42(7):2969-2973. doi: 10.1007/s10072-021-05117-1. Epub 2021 Feb 9.
Neurol Sci. 2021.
PMID: 33559790
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A novel PSEN2 p.Ser175Phe variant in a family with Alzheimer's disease.
Guven G, Samanci B, Gulec C, Hanagasi H, Gurvit H, Gokalp EE, Tepgec F, Guler S, Uyguner O, Bilgic B.
Guven G, et al. Among authors: gokalp ee.
Neurol Sci. 2021 Jun;42(6):2497-2504. doi: 10.1007/s10072-021-05243-w. Epub 2021 Apr 15.
Neurol Sci. 2021.
PMID: 33855622
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