ID   GM02421
AC   CVCL_H182
SY   GM 2421; GM02421A
DR   CLO; CLO_0033092
DR   BioSample; SAMN00807753
DR   Coriell; GM02421
DR   Wikidata; Q54837475
RX   CelloPub=CLPUB00447;
RX   PubMed=6617268;
RX   PubMed=6661932;
CC   Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   16FW
CA   Finite cell line
DT   Created: 11-02-13; 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 misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992).
//
RX   PubMed=6617268; DOI=10.1159/000131883;
RA   Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.;
RT   "Breakpoint map of chromosomal inversion and deletion cell cultures in
RT   the NIGMS Human Genetic Mutant Cell Repository.";
RL   Cytogenet. Cell Genet. 35:298-302(1983).
//
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).
//