ID   18T-iPSC
AC   CVCL_VK55
DR   Wikidata; Q93300538
RX   PubMed=29862150;
CC   From: Key Laboratory for Rare Disease Research of Shandong Province; Jinan; China.
CC   Omics: Transcriptomics; RNAseq.
CC   Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
DI   NCIt; C36626; Trisomy 18
DI   ORDO; Orphanet_3380; Trisomy 18
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   Fetus
CA   Induced pluripotent stem cell
DT   Created: 07-09-18; Last updated: 10-04-25; Version: 6
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RX   PubMed=29862150; DOI=10.5582/irdr.218.01038; PMCID=PMC5982630;
RA   Xing K.-X., Cui Y.-Z., Luan J., Zhou X.-Y., Shi L., Han J.-X.;
RT   "Establishment of a human trisomy 18 induced pluripotent stem cell
RT   line from amniotic fluid cells.";
RL   Intractable Rare Dis. Res. 7:94-99(2018).
//