ID   GM01663
AC   CVCL_V810
SY   GM-1663; GM 1663; GM1663
DR   CLO; CLO_0030957
DR   BioSample; SAMN00807049
DR   Coriell; GM01663
DR   Wikidata; Q54836995
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=761481;
RX   PubMed=6661932;
RX   PubMed=7329430;
RX   PubMed=7471105;
CC   Population: Caucasian.
CC   Karyotypic information: 46,XY,der(17)(17qter->17p13::13q14->13qter)mat (Coriell=GM01663).
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   14Y
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=761481; DOI=10.1159/000131318;
RA   Schinzel A., Aronson M.M., Greene A.E., Coriell L.L.;
RT   "Partial trisomy for the distal long arm of chromosome 13, 46,XY.
RT   Repository identification No. GM-1663.";
RL   Cytogenet. Cell Genet. 23:148-148(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).
//
RX   PubMed=7329430; DOI=10.1016/0027-5107(81)90059-2;
RA   Nove J., Nichols W.W., Weichselbaum R.R., Little J.B.;
RT   "Abnormalities of human chromosome 13 and in vitro radiosensitivity; a
RT   study of 19 fibroblast strains.";
RL   Mutat. Res. 84:157-167(1981).
//
RX   PubMed=7471105;
RA   Weichselbaum R.R., Nove J., Little J.B.;
RT   "X-ray sensitivity of fifty-three human diploid fibroblast cell
RT   strains from patients with characterized genetic disorders.";
RL   Cancer Res. 40:920-925(1980).
//