ID   GM04370
AC   CVCL_X304
SY   GM 4370; GM04370A
DR   CLO; CLO_0019310
DR   Coriell; GM04370
DR   Wikidata; Q54838501
RX   CelloPub=CLPUB00447;
RX   PubMed=6661932;
RX   PubMed=10577914;
CC   Population: Caucasian.
CC   Karyotypic information: 47,XX,+der(22)(22pter->22q11::11q23->11qter)mat (Coriell=GM04370).
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C84392; Mental retardation
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   4Y
CA   Finite cell line
DT   Created: 17-07-14; 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=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=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).
//