ID   GM05009
AC   CVCL_X315
SY   GM 5009; GM05009B
DR   CLO; CLO_0025671
DR   Coriell; GM05009
DR   Wikidata; Q54838808
RX   CelloPub=CLPUB00447;
RX   PubMed=6661932;
CC   Population: Caucasian.
CC   Karyotypic information: 49,XXXXX [31]; 48,XXXX [15]; 48,XXXX,t(1;18)(1qter->1p36::18q21->18qter;18pter->18q21::1p36->1pter) [2]; 49,XXXXX,t(1;18)(1qter->1p36::18q21->18qter;18pter->18q21::1p36->1pter) [2] (Coriell=GM05009).
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C89802; Penta X syndrome
DI   ORDO; Orphanet_11; Pentasomy X
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   6M
CA   Finite cell line
DT   Created: 17-07-14; Last updated: 29-06-23; Version: 8
//
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   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).
//