ID   GM07215
AC   CVCL_2Y98
DR   CLO; CLO_0036922
DR   Coriell; GM07215
DR   Wikidata; Q54842582
RX   CelloPub=CLPUB00447;
RX   PubMed=23665875;
CC   Population: Caucasian.
CC   Omics: Variations; CNV analysis.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C2989; 22q11.2 deletion syndrome
DI   ORDO; Orphanet_567; 22q11.2 deletion syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   3D
CA   Finite cell line
DT   Created: 22-09-15; Last updated: 10-04-25; Version: 11
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RX   PubMed=23665875; DOI=10.1534/g3.113.006577; PMCID=PMC3704242;
RA   Tang, Zhen-Ya
RA   Berlin, Dorit S.
RA   Toji, Lorraine Hellenga
RA   Toruner, Gokce Altay
RA   Beiswanger, Christine M.
RA   Kulkarni, Shashikant
RA   Martin, Christa Lese
RA   Emanuel, Beverly S.
RA   Christman, Michael Fabrique
RA   Gerry, Norman Phillip
RT   "A dynamic database of microarray-characterized cell lines with
RT   various cytogenetic and genomic backgrounds.";
RL   G3 (Bethesda) 3:1143-1149(2013).
//
RX   CelloPub=CLPUB00447;
RA   Mulivor, Richard A.
RA   Suchy, Sharon F.
RT   "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 16th edition. October 1992.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992).
//