ID   HPS1627
AC   CVCL_YS36
AS   CVCL_C0HH
SY   BRCi019-A
DR   hPSCreg; BRCi019-A
DR   RCB; HPS1627
DR   Wikidata; Q94219799
RX   PubMed=35292424;
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C2989; 22q11.2 deletion syndrome
DI   ORDO; Orphanet_567; 22q11.2 deletion syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_YS37 ! HPS1628
OI   CVCL_YS38 ! HPS1629
OI   CVCL_YS39 ! HPS1630
OI   CVCL_YS40 ! HPS1631
SX   Female
AG   <10Y
CA   Induced pluripotent stem cell
DT   Created: 12-03-20; Last updated: 29-06-23; Version: 6
//
RX   PubMed=35292424; DOI=10.1016/j.scr.2022.102744;
RA   Shimizu T., Matsuo-Takasaki M., Luijkx D., Takami M., Arai Y.,
RA   Noguchi M., Nakamura Y., Hayata T., Saito M.K., Hayashi Y.;
RT   "Generation of human induced pluripotent stem cell lines derived from
RT   four DiGeorge syndrome patients with 22q11.2 deletion.";
RL   Stem Cell Res. 61:102744-102744(2022).
//