Publication
| Wilson PF, Nham PB, Urbin SS, Hinz JM, Jones IM, Thompson LH, Inter-individual variation in DNA double-strand break repair in human fibroblasts before and after exposure to low doses of ionizing radiation Mutation research683:91-7 2009 |
| PubMed ID: 19896956 |
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| Records Return:
(10)
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| Catalog ID | Gender | Age at Sampling | Family | Relationship | Description | Collection_Type_id |
| GM05823 | Male | 18 YR | 868 | proband | ATAXIA-TELANGIECTASIA; AT | GM |
| GM03487 | Male | 8 YR | 516 | proband | ATAXIA-TELANGIECTASIA; AT | GM |
| GM18366 | Male | 6 YR | 3302 | proband | SECKEL SYNDROME | GM |
| GM07166 | Female | 20 YR | 2100 | proband | NIJMEGEN BREAKAGE SYNDROME | GM |
| GM16096 | Female | 18 YR | 1876 | proband | IMMUNODEFICIENCY 96; IMD96 | GM |
| GM16088 | Male | 15 YR | 1872 | proband | LIG4 SYNDROME | GM |
| GM09812 | Female | 15 YR | 1124 | proband | SECKEL SYNDROME | GM |
| GM02052 | Female | 15 YR | | proband | ATAXIA-TELANGIECTASIA; AT | GM |
| GM17523 | Female | 10 YR | | proband | LIG4 SYNDROME | GM |
| GM02361 | Male | 14 YR | | proband | FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG | GM |
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