ID   GM00217
AC   CVCL_V758
SY   GM-217; GM-0217; GM 217
DR   Coriell; GM00217
DR   Wikidata; Q54836096
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=1132255;
RX   PubMed=6661932;
CC   Discontinued: Coriell; GM00217; probable.
CC   Cell type: Fibroblast; CL=CL_0000057.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   9D
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 8
//
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 misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977).
//
RX   PubMed=1132255; DOI=10.1159/000130327;
RA   Zackai E.H., Mellman W.J., Aronson M.M., Miller R.C., Greene A.E.,
RA   Coriell L.L.;
RT   "A (10;17) translocation, unbalanced, 46 chromosomes. Repository
RT   identification No. GM-217.";
RL   Cytogenet. Cell Genet. 14:90-91(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).
//