ID   GM10649
AC   CVCL_UR80
DR   Coriell; GM10649
DR   Wikidata; Q93810070
RX   CelloPub=CLPUB00447;
RX   PubMed=1897572;
CC   Discontinued: Coriell; GM10649; probable.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C84978; Osteochondrodysplasia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   3D
CA   Finite cell line
DT   Created: 25-02-19; Last updated: 29-06-23; Version: 5
//
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 misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992).
//
RX   PubMed=1897572; DOI=10.1002/ajmg.1320400212;
RA   Faye-Petersen O.M., Ward K., Carey J.C., Knisely A.S.;
RT   "Osteochondrodysplasia with rhizomelia, platyspondyly, callosal
RT   agenesis, thrombocytopenia, hydrocephalus, and hypertension.";
RL   Am. J. Med. Genet. 40:183-187(1991).
//