ID   GM03372
AC   CVCL_2S90
DR   CLO; CLO_0016662
DR   BioSample; SAMN00808377
DR   Coriell; GM03372
DR   Wikidata; Q54838034
RX   CelloPub=CLPUB00447;
RX   PubMed=10577914;
CC   Population: African American.
CC   Karyotypic information: 46,XX,t(11;22)(11pter->11q23::22q11->22qter;22pter->22q11::11q23->11qter) (Coriell=GM03372).
CC   Cell type: Fibroblast; CL=CL_0000057.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   28Y
CA   Finite cell line
DT   Created: 22-09-15; Last updated: 29-06-23; Version: 9
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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=10577914; DOI=10.1086/302689; PMCID=PMC1288371;
RA   Edelmann L.J., Spiteri E., McCain N., Goldberg R., Pandita R.K.,
RA   Duong S., Fox J.E., Blumenthal D., Lalani S.R., Shaffer L.G.,
RA   Morrow B.E.;
RT   "A common breakpoint on 11q23 in carriers of the constitutional
RT   t(11;22) translocation.";
RL   Am. J. Hum. Genet. 65:1608-1616(1999).
//