ID   GM10381
AC   CVCL_N351
DR   CLO; CLO_0028573
DR   BioSample; SAMN00799969
DR   Coriell; GM10381
DR   Wikidata; Q54844423
RX   CelloPub=CLPUB00447;
CC   Population: African American.
CC   Derived from site: In situ; Fetus; UBERON=UBERON_0000323.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C118436; Fraser syndrome
DI   ORDO; Orphanet_2052; Fraser syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_N350 ! GM10379
SX   Male
AG   19FW
CA   Finite cell line
DT   Created: 05-11-13; Last updated: 29-06-23; Version: 11
//
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).
//