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Cellosaurus GM01993 (CVCL_F023)

[Text version]
Cell line name GM01993
Synonyms GM-1993; GM 1993
Accession CVCL_F023
Resource Identification Initiative To cite this cell line use: GM01993 (RRID:CVCL_F023)
Comments Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
Disease 47,XYY syndrome (NCIt: C85237)
47,XYY syndrome (ORDO: Orphanet_8)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 21FW
Category Finite cell line
Publications

DOI=10.5962/bhl.title.4090
Coriell L.L., Greene A.E.
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 4th edition. October 1977.
(In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977)

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; GM01993
Cell line databases/resources CLO; CLO_0032354
Biological sample resources BioSample; SAMN00807358
Encyclopedic resources Wikidata; Q54837219
Entry history
Entry creation22-Oct-2012
Last entry update29-Jun-2023
Version number14