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Whole exome sequencing identified a homozygous novel variant in CEP290 gene causes Meckel syndrome.
J Cell Mol Med. 2020 Jan;24(2):1906-1916. doi: 10.1111/jcmm.14887. Epub 2019 Dec 15.
J Cell Mol Med. 2020.
PMID: 31840411
Free PMC article.
Whole exome sequencing identified a homozygous novel mutation in SUOX gene causes extremely rare autosomal recessive isolated sulfite oxidase deficiency.
Zhang R, Hao Y, Xu Y, Qin J, Wang Y, Kumar Dey S, Li C, Wang H, Banerjee S.
Zhang R, et al. Among authors: kumar dey s.
Clin Chim Acta. 2022 Jul 1;532:115-122. doi: 10.1016/j.cca.2022.06.005. Epub 2022 Jun 6.
Clin Chim Acta. 2022.
PMID: 35679912
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Telomere length analysis in Down syndrome birth.
Bhaumik P, Bhattacharya M, Ghosh P, Ghosh S, Kumar Dey S.
Bhaumik P, et al. Among authors: kumar dey s.
Mech Ageing Dev. 2017 Jun;164:20-26. doi: 10.1016/j.mad.2017.03.006. Epub 2017 Mar 19.
Mech Ageing Dev. 2017.
PMID: 28327364
Clinical Trial.
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Telomere Length Inheritance and Shortening in Trisomy 21.
Bhattacharya M, Bhaumik P, Ghosh P, Majumder P, Kumar Dey S.
Bhattacharya M, et al. Among authors: kumar dey s.
Fetal Pediatr Pathol. 2020 Oct;39(5):390-400. doi: 10.1080/15513815.2019.1661049. Epub 2019 Sep 13.
Fetal Pediatr Pathol. 2020.
PMID: 31514556
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Telomere length comparison between oral cells and blood cells among neonates.
Bhattacharya M, Bhaumik P, Kumar-Dey S.
Bhattacharya M, et al. Among authors: kumar dey s.
Turk J Pediatr. 2019;61(4):520-524. doi: 10.24953/turkjped.2019.04.008.
Turk J Pediatr. 2019.
PMID: 31990469
Free article.
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18F-FDG-induced DNA damage, chromosomal aberrations, and toxicity in V79 lung fibroblast cells.
Mondal T, Nautiyal A, Agrawal M, Mitra D, Goel A, Kumar Dey S.
Mondal T, et al. Among authors: kumar dey s.
Mutat Res Genet Toxicol Environ Mutagen. 2019 Nov;847:503105. doi: 10.1016/j.mrgentox.2019.503105. Epub 2019 Oct 11.
Mutat Res Genet Toxicol Environ Mutagen. 2019.
PMID: 31699341
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