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TET2 rs1548483 SNP Associating with Susceptibility to Molecularly Annotated Polycythemia Vera and Primary Myelofibrosis.
J Pers Med. 2020 Dec 1;10(4):259. doi: 10.3390/jpm10040259.
J Pers Med. 2020.
PMID: 33271790
Free PMC article.
Association Analysis of TP53 rs1042522, MDM2 rs2279744, rs3730485, MDM4 rs4245739 Variants and Acute Myeloid Leukemia Susceptibility, Risk Stratification Scores, and Clinical Features: An Exploratory Study.
Tripon F, Iancu M, Trifa A, Crauciuc GA, Boglis A, Balla B, Cosma A, Dima D, Candea M, Lazar E, Jimbu L, Banescu C.
Tripon F, et al. Among authors: cosma a.
J Clin Med. 2020 Jun 1;9(6):1672. doi: 10.3390/jcm9061672.
J Clin Med. 2020.
PMID: 32492903
Free PMC article.
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Exon 21 deletion in the OPHN1 gene in a family with syndromic X-linked intellectual disability: Case report.
Bogliş A, Cosma AS, Tripon F, Bãnescu C.
Bogliş A, et al. Among authors: cosma as.
Medicine (Baltimore). 2020 Aug 14;99(33):e21632. doi: 10.1097/MD.0000000000021632.
Medicine (Baltimore). 2020.
PMID: 32872024
Free PMC article.
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