ID   GM00627
AC   CVCL_M978
SY   GM-627; GM17151
DR   CLO; CLO_0013957
DR   CLO; CLO_0028869
DR   Coriell; GM00627
DR   Coriell; GM17151
DR   GEO; GSM924661
DR   Wikidata; Q54836353
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=1225502;
CC   Part of: Human variation panel.
CC   Population: African American.
CC   Karyotypic information: 46,XX,t(13;22)(13pter->13q22::22q13->22qter;22pter->22q13::13q22->13qter) (Coriell=GM00627).
CC   Omics: DNA methylation analysis.
CC   Cell type: Fibroblast; CL=CL_0000057.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   30Y
CA   Finite cell line
DT   Created: 05-11-13; Last updated: 29-06-23; Version: 12
//
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=1225502; DOI=10.1159/000130542;
RA   Kim H.J., Hirschhorn K., Hsu L.Y.-F., Aronson M.M., Greene A.E.,
RA   Coriell L.L.;
RT   "A (13;22) translocation, 46 chromosomes. Repository identification
RT   No. GM-627.";
RL   Cytogenet. Cell Genet. 15:406-407(1975).
//