ID   GM01570
AC   CVCL_V809
SY   GM-1570; GM 1570
DR   CLO; CLO_0031453
DR   Coriell; GM01570
DR   Wikidata; Q54836917
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=446098;
RX   PubMed=6661932;
CC   Karyotypic information: 6,XY,rec(13)(pter->q22::p11->pter)pat (Coriell=GM01570).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   16FW
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 misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (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 misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977).
//
RX   PubMed=446098; DOI=10.1159/000131341;
RA   Seabright M., Gregson N., Aronson M.M., Greene A.E., Coriell L.L.;
RT   "Recombinant chromosome 13 with a duplication of a short arm.
RT   Repository identification No. GM-1570.";
RL   Cytogenet. Cell Genet. 23:281-281(1979).
//
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).
//