Publication
| Prince PR, Ogburn CE, Moser MJ, Emond MJ, Martin GM, Monnat RJ Jr, Cell fusion corrects the 4-nitroquinoline 1-oxide sensitivity of Werner syndrome fibroblast cell lines. Hum Genet105:132-8 1999 |
| PubMed ID: 10480367 |
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| Records Return:
(10)
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| Catalog ID | Gender | Age at Sampling | Family | Relationship | Description | Collection_Type_id |
| GM06914 | Male | 12 YR | 969 | proband | FANCONI ANEMIA, COMPLEMENTATION GROUP A; FANCA | GM |
| GM05849 | Male | 18 YR | 868 | proband | ATAXIA-TELANGIECTASIA; AT | GM |
| GM00847 | Male | 5 YR | 71 | maternal cousin | LESCH-NYHAN SYNDROME; LNS | GM |
| GM04312 | Female | 7 YR | 695 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA | GM |
| GM04429 | Female | 7 YR | 484 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA | GM |
| GM00638 | Male | 3 MO | 27 | proband | GALACTOSEMIA | GM |
| GM08505 | Female | 27 YR | 2061 | proband | BLOOM SYNDROME; BLM | GM |
| GM08437 | Female | 64 YR | 2047 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF | GM |
| GM00637 | Female | 18 YR | 162 | proband | SV40 VIRUS-TRANSFORMED APPARENTLY HEALTHY CULTURE | GM |
| GM08207 | Female | 19 YR | 1212 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD | GM |
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