ID   GM02668
AC   CVCL_X093
SY   GM 2668
DR   CLO; CLO_0014999
DR   Coriell; GM02668
DR   Wikidata; Q54837612
RX   CelloPub=CLPUB00447;
RX   PubMed=6617268;
RX   PubMed=6661932;
CC   Population: Caucasian.
CC   Karyotypic information: 46,X,del(Y)(pter->q11.2) [77%]; 45,X [33%] (Coriell=GM02668).
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C26900; Turner syndrome
DI   ORDO; Orphanet_881; Turner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Sex ambiguous
AG   41Y
CA   Finite cell line
DT   Created: 17-07-14; Last updated: 05-10-23; Version: 11
//
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=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).
//