ID   SDQLCHi065-A
AC   CVCL_D4ZN
DR   BioSamples; SAMEA115174033
DR   hPSCreg; SDQLCHi065-A
DR   Wikidata; Q127384267
RX   PubMed=38377649;
CC   From: Qilu Children's Hospital of Shandong University; Jinan; China.
CC   Population: Chinese; Han.
CC   Karyotypic information: 47,XY,+21,inv(9)(p12;q21),16qh+ (PubMed=38377649).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C2993; Down syndrome
DI   ORDO; Orphanet_870; Down syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   8D
CA   Induced pluripotent stem cell
DT   Created: 02-05-24; Last updated: 10-09-24; Version: 2
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RX   PubMed=38377649; DOI=10.1016/j.scr.2024.103351;
RA   Zhang X., Xin H.-M., Liu Y., Gai Z.-T., Li Z.-L.;
RT   "An integration-free iPSC line SDQLCHi065-A from a patient with down
RT   syndrome, possessing a 47, XY,+21, inv(9)(p12q21),16qh + karyotype.";
RL   Stem Cell Res. 76:103351-103351(2024).
//