ID   GM00088
AC   CVCL_X224
SY   GM-88; GM-0088; GM0088; GM 88
DR   CLO; CLO_0025156
DR   Coriell; GM00088
DR   Wikidata; Q54836029
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=4780774;
RX   PubMed=6661932;
RX   PubMed=10377420;
RX   PubMed=23665875;
CC   Population: Caucasian.
CC   Karyotypic information: 46,X,i(X)(p11.21) (PubMed=10377420).
CC   Omics: CNV analysis.
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   Female
AG   19Y
CA   Finite cell line
DT   Created: 17-07-14; Last updated: 29-06-23; Version: 15
//
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=4780774; DOI=10.1159/000130478;
RA   Borgaonkar D.S.;
RT   "An X,isochromosome X (long arm), 46 chromosomes. Human Genetic Mutant
RT   Cell Repository, Camden, N.J., identification No. GM-88.";
RL   Cytogenet. Cell Genet. 12:372-373(1973).
//
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=10377420; DOI=10.1073/pnas.96.13.7364;
RA   Carrel L., Willard H.F.;
RT   "Heterogeneous gene expression from the inactive X chromosome: an
RT   X-linked gene that escapes X inactivation in some human cell lines but
RT   is inactivated in others.";
RL   Proc. Natl. Acad. Sci. U.S.A. 96:7364-7369(1999).
//
RX   PubMed=23665875; DOI=10.1534/g3.113.006577;
RA   Tang Z.-Y., Berlin D.S., Toji L.H., Toruner G.A., Beiswanger C.M.,
RA   Kulkarni S., Martin C.L., Emanuel B.S., Christman M., Gerry N.P.;
RT   "A dynamic database of microarray-characterized cell lines with
RT   various cytogenetic and genomic backgrounds.";
RL   G3 (Bethesda) 3:1143-1149(2013).
//