ID   GM03767
AC   CVCL_X111
SY   GM 3767
DR   CLO; CLO_0015491
DR   BioSample; SAMN00808521
DR   Coriell; GM03767
DR   Wikidata; Q54838222
RX   CelloPub=CLPUB00447;
RX   PubMed=6617268;
RX   PubMed=6661932;
CC   Population: Caucasian.
CC   Karyotypic information: 46,XY,del(18)(qter->p11) (Coriell=GM03767).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C84521; Deletion 18p syndrome
DI   ORDO; Orphanet_1598; Monosomy 18p
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   3Y
CA   Finite cell line
DT   Created: 17-07-14; 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=6617268; DOI=10.1159/000131883;
RA   Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.;
RT   "Breakpoint map of chromosomal inversion and deletion cell cultures in
RT   the NIGMS Human Genetic Mutant Cell Repository.";
RL   Cytogenet. Cell Genet. 35:298-302(1983).
//
RX   PubMed=6661932; DOI=10.1159/000131990;
RA   Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.;
RT   "Chromosome maps of cell lines with specific monosomic or trisomic
RT   portions of the genome in the NIGMS Human Genetic Mutant Cell
RT   Repository.";
RL   Cytogenet. Cell Genet. 36:652-658(1983).
//