ID   GM10879
AC   CVCL_AD74
DR   CLO; CLO_0024119
DR   BioSample; SAMN00800308
DR   Coriell; GM10879
DR   Wikidata; Q54844713
RX   CelloPub=CLPUB00447;
CC   Population: Caucasian.
CC   Derived from site: In situ; Fetus; UBERON=UBERON_0000323.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C98932; Fryns syndrome
DI   ORDO; Orphanet_2059; Fryns syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   27FW
CA   Finite cell line
DT   Created: 23-02-16; Last updated: 29-06-23; Version: 8
//
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).
//