ID   GM50113
AC   CVCL_0F90
SY   JL143
DR   CLO; CLO_0014755
DR   Coriell; GM50113
DR   Wikidata; Q54854201
RX   PubMed=8488839;
RX   PubMed=23665875;
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Omics: CNV analysis.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C84522; Deletion 18q syndrome
DI   ORDO; Orphanet_1600; Monosomy 18q
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   Age unspecified
CA   Transformed cell line
DT   Created: 10-04-15; Last updated: 29-06-23; Version: 11
//
RX   PubMed=8488839;
RA   Kline A.D., White M.E., Wapner R.J., Rojas K., Biesecker L.G.,
RA   Kamholz J., Zackai E.H., Muenke M., Scott C.I. Jr., Overhauser J.;
RT   "Molecular analysis of the 18q- syndrome -- and correlation with
RT   phenotype.";
RL   Am. J. Hum. Genet. 52:895-906(1993).
//
RX   PubMed=23665875; DOI=10.1534/g3.113.006577;
RA   Tang Z.-Y., Berlin D.S., Toji L.H., Toruner G.A., Beiswanger C.M.,
RA   Kulkarni S., Martin C.L., Emanuel B.S., Christman M., Gerry N.P.;
RT   "A dynamic database of microarray-characterized cell lines with
RT   various cytogenetic and genomic backgrounds.";
RL   G3 (Bethesda) 3:1143-1149(2013).
//