ID   GM00098
AC   CVCL_V748
SY   GM-98; GM-0098; GM 98
DR   CLO; CLO_0025820
DR   Coriell; GM00098
DR   Wikidata; Q54836040
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=1149496;
RX   PubMed=6661932;
CC   Karyotypic information: 46,XY,der(21)(21qter->21p12::4p11->4pter)mat (Coriell=GM00098).
CC   Cell type: Fibroblast; CL=CL_0000057.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   10M
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 10
//
RX   CelloPub=CLPUB00447;
RA   Mulivor R.A., Suchy S.F.;
RT   "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 16th edition. October 1992.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992).
//
RX   DOI=10.5962/bhl.title.4090;
RA   Coriell L.L., Greene A.E.;
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 4th edition. October 1977.";
RL   (In) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (1977).
//
RX   PubMed=1149496; DOI=10.1159/000130335;
RA   Seabright M., Miller R.C., Greene A.E., Coriell L.L.;
RT   "A (4;21) translocation, unbalanced, 46 chromosomes. Repository
RT   identification No. GM-98.";
RL   Cytogenet. Cell Genet. 14:152-153(1975).
//
RX   PubMed=6661932; DOI=10.1159/000131990;
RA   Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.;
RT   "Chromosome maps of cell lines with specific monosomic or trisomic
RT   portions of the genome in the NIGMS Human Genetic Mutant Cell
RT   Repository.";
RL   Cytogenet. Cell Genet. 36:652-658(1983).
//