ID   Cri du Chat
AC   CVCL_4150
AS   CVCL_X223
SY   GM00071; GM-0071; GM-71; GM 71; GM71
DR   CLO; CLO_0002611
DR   CLO; CLO_0025165
DR   CLDB; cl910
DR   ATCC; CCL-90
DR   BioSample; SAMN03471291
DR   Coriell; GM00071
DR   ECACC; 90102533
DR   KCB; KCB 94023YJ
DR   Wikidata; Q54814486
RX   CelloPub=CLPUB00447;
RX   DOI=10.1007/BF02618370;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=1001031;
RX   PubMed=6661932;
RX   PubMed=6988327;
CC   Population: Caucasian.
CC   Discontinued: ECACC; 90102533; probable.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): ATCC=CCL-90
ST   Amelogenin: X
ST   CSF1PO: 10,12
ST   D13S317: 11
ST   D16S539: 11,12
ST   D18S51: 16,18
ST   D19S433: 14,15
ST   D21S11: 30
ST   D2S1338: 20,23
ST   D3S1358: 16,17
ST   D5S818: 10,11
ST   D7S820: 8,11
ST   D8S1179: 13
ST   FGA: 21,22
ST   Penta D: 10,11
ST   Penta E: 7,13
ST   TH01: 9.3
ST   TPOX: 8
ST   vWA: 15,16
DI   NCIt; C34518; Cri du chat syndrome
DI   ORDO; Orphanet_281; Monosomy 5p
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   19Y
CA   Finite cell line
DT   Created: 04-04-12; Last updated: 02-05-24; Version: 21
//
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=10.1007/BF02618370;
RA   Stulberg C.S., Coriell L.L., Kniazeff A.J., Shannon J.E.;
RT   "The animal cell culture collection.";
RL   In Vitro 5:1-16(1970).
//
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=1001031; DOI=10.1159/000130718;
RA   Breg W.R., Aronson M.M., Greene A.E., Coriell L.L.;
RT   "Deletion of the short arm of chromosome 5 from a subject with
RT   cri-du-chat syndrome. Repository identification No. GM-71.";
RL   Cytogenet. Cell Genet. 17:239-240(1976).
//
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).
//
RX   PubMed=6988327; DOI=10.1007/BF02831503;
RA   O'Brien S.J., Shannon J.E., Gail M.H.;
RT   "A molecular approach to the identification and individualization of
RT   human and animal cells in culture: isozyme and allozyme genetic
RT   signatures.";
RL   In Vitro 16:119-135(1980).
//