ID   GM03809
AC   CVCL_JE58
SY   GM3809
DR   CLO; CLO_0015559
DR   BioSample; SAMN00808542
DR   Coriell; GM03809
DR   Wikidata; Q54838246
RX   CelloPub=CLPUB00447;
RX   PubMed=2570029;
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C3718; Wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome
DI   ORDO; Orphanet_893; WAGR syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   2Y
CA   Finite cell line
DT   Created: 15-05-17; 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=2570029; DOI=10.1016/0888-7543(89)90084-0;
RA   Gessler M., Bruns G.A.P.;
RT   "A physical map around the WAGR complex on the short arm of chromosome
RT   11.";
RL   Genomics 5:43-55(1989).
//