ID   GM03913
AC   CVCL_1K35
SY   GM03913A
DR   CLO; CLO_0016129
DR   Coriell; GM03913
DR   Wikidata; Q54838320
RX   CelloPub=CLPUB00447;
RX   PubMed=10655550;
CC   Population: Caucasian; French Canadian.
CC   Karyotypic information: 46,XY [46%]; 47,XY,+7 [54%] (Coriell=GM03913).
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C4681; Roberts-SC phocomelia syndrome
DI   ORDO; Orphanet_3103; Roberts syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   1Y8M
CA   Finite cell line
DT   Created: 08-07-15; 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=10655550; DOI=10.1093/hmg/9.3.403;
RA   Ouellette M.M., McDaniel L.D., Wright W.E., Shay J.W., Schultz R.A.;
RT   "The establishment of telomerase-immortalized cell lines representing
RT   human chromosome instability syndromes.";
RL   Hum. Mol. Genet. 9:403-411(2000).
//