ID   GM01322
AC   CVCL_AB28
SY   GM-1322; GM 1322
DR   CLO; CLO_0030911
DR   BioSample; SAMN00803800
DR   Coriell; GM01322
DR   Wikidata; Q54836765
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=6156493;
CC   Population: African American.
CC   Karyotypic information: 68,XX [1]; 69,XXY [49] (Coriell=GM01322).
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C85204; Triploidy syndrome
DI   ORDO; Orphanet_3376; Triploidy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Sex ambiguous
AG   2D
CA   Finite cell line
DT   Created: 23-02-16; Last updated: 29-06-23; Version: 9
//
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   DOI=10.5962/bhl.title.4090;
RA   Coriell L.L., Greene A.E.;
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 4th edition. October 1977.";
RL   (In) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (1977).
//
RX   PubMed=6156493; DOI=10.1007/BF01538795;
RA   Willard H.F., Breg W.R.;
RT   "Human X chromosomes: synchrony of DNA replication in diploid and
RT   triploid fibroblasts with multiple active or inactive X chromosomes.";
RL   Somatic Cell Genet. 6:187-198(1980).
//