ID   GM03769
AC   CVCL_X299
SY   GM 3769
DR   CLO; CLO_0015492
DR   BioSample; SAMN00808522
DR   Coriell; GM03769
DR   Wikidata; Q54838224
RX   CelloPub=CLPUB00447;
RX   PubMed=6661932;
CC   Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
DI   NCIt; C36626; Trisomy 18
DI   ORDO; Orphanet_3380; Trisomy 18
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   16FW
CA   Finite cell line
DT   Created: 17-07-14; Last updated: 29-06-23; Version: 10
//
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=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).
//