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Cellosaurus GM03769 (CVCL_X299)

[Text version]
Cell line name GM03769
Synonyms GM 3769
Accession CVCL_X299
Resource Identification Initiative To cite this cell line use: GM03769 (RRID:CVCL_X299)
Comments Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
Disease Trisomy 18 (NCIt: C36626)
Trisomy 18 (ORDO: Orphanet_3380)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 16FW
Category Finite cell line
Publications

PubMed=6661932; DOI=10.1159/000131990
Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.
Chromosome maps of cell lines with specific monosomic or trisomic portions of the genome in the NIGMS Human Genetic Mutant Cell Repository.
Cytogenet. Cell Genet. 36:652-658(1983)

CLPUB00447
Mulivor R.A., Suchy S.F.
1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992.
(In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992)

Cross-references
Cell line collections (Providers) Coriell; GM03769
Cell line databases/resources CLO; CLO_0015492
Biological sample resources BioSample; SAMN00808522
Encyclopedic resources Wikidata; Q54838224
Entry history
Entry creation17-Jul-2014
Last entry update29-Jun-2023
Version number10