PubMed=1183234; DOI=10.1159/000130500
Aronson M.M., Zackai E.H., Mellman W.J., Miller R.C., Greene A.E., Coriell L.L.
A (13) terminal deletion, 46 chromosomes. Repository identification No. GM-250.
Cytogenet. Cell Genet. 15:57-58(1975)

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) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (1977)

PubMed=7471105
Weichselbaum R.R., Nove J., Little J.B.
X-ray sensitivity of fifty-three human diploid fibroblast cell strains from patients with characterized genetic disorders.
Cancer Res. 40:920-925(1980)

PubMed=7329430; DOI=10.1016/0027-5107(81)90059-2
Nove J., Nichols W.W., Weichselbaum R.R., Little J.B.
Abnormalities of human chromosome 13 and in vitro radiosensitivity; a study of 19 fibroblast strains.
Mutat. Res. 84:157-167(1981)

PubMed=6617268; DOI=10.1159/000131883
Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.
Breakpoint map of chromosomal inversion and deletion cell cultures in the NIGMS Human Genetic Mutant Cell Repository.
Cytogenet. Cell Genet. 35:298-302(1983)

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) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992)