ID   GM04188
AC   CVCL_1H83
DR   CLO; CLO_0015927
DR   Coriell; GM04188
DR   Wikidata; Q54838400
RX   CelloPub=CLPUB00447;
RX   PubMed=6316146;
CC   Population: Caucasian.
CC   Karyotypic information: 46,XX,t(6;19)(6pter->6q13::19p13.3->19pter;19qter->19p13.3::6q13->6qter) [8]; 46,XX,t(7;22)(7qter->7p15::22q13->22qter;22pter->22q13::7p15>-7pter),del(qter->12)(p13) [4]; 46,XX [38] (Coriell=GM04188).
CC   Cell type: Fibroblast; CL=CL_0000057.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_1H84 ! GM04189
SX   Female
AG   77Y
CA   Finite cell line
DT   Created: 08-07-15; Last updated: 29-06-23; Version: 9
//
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 misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992).
//
RX   PubMed=6316146; DOI=10.1038/306234a0;
RA   Gusella J.F., Wexler N.S., Conneally P.M., Naylor S.L., Anderson M.A.,
RA   Tanzi R.E., Watkins P.C., Ottina K., Wallace M.R., Sakaguchi A.Y.,
RA   Young A.B., Shoulson I., Bonilla E., Martin J.B.;
RT   "A polymorphic DNA marker genetically linked to Huntington's
RT   disease.";
RL   Nature 306:234-238(1983).
//