Publication
| Nouspikel T, Lalle P, Leadon SA, Cooper PK, Clarkson SG, A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function. Proc Natl Acad Sci U S A94:3116-21 1997 |
| PubMed ID: 9096355 |
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| Records Return:
(3)
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| Catalog ID | Gender | Age at Sampling | Family | Relationship | Description | Collection_Type_id |
| GM13371 | Female | 5 YR | 1849 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG | GM |
| GM13370 | Male | 2 YR | 1848 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG | GM |
| GM00038 | Female | 9 YR | 163 | daughter | APPARENTLY HEALTHY INDIVIDUAL | GM |
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