Publication
Moriwaki S, Stefanini M, Lehmann AR, Hoeijmakers JH, Robbins JH, Rapin I, Botta E, Tanganelli B, Vermeulen W, Broughton BC, Kraemer KH, DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and cockayne syndrome resemble xeroderma pigmentosum cells. J Invest Dermatol107(4):647-53 1996 |
PubMed ID: 8823375 |
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Records Return:
(14)
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Catalog ID | Gender | Age at Sampling | Family | Relationship | Description | Collection_Type_id |
GM03248 | Male | 5 YR | 714 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD | GM |
GM02415 | Female | 34 YR | 626 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E | GM |
GM02250 | Female | 17 YR | 484 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA | GM |
GM05509 | Female | 17 YR | 484 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA | GM |
GM03651 | Female | 25 YR | 3029 | proband | APPARENTLY HEALTHY INDIVIDUAL | GM |
AG08805 | Female | 37 YR | 2093 | mother | COCKAYNE SYNDROME TYPE A - 216400 | AG |
AG08807 | Male | 37 YR | 2093 | father | COCKAYNE SYNDROME TYPE A - 216400 | AG |
AG08802 | Male | 1 YR | 2093 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG | AG |
AG08803 | Male | 1 YR | 2093 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG | AG |
GM04313 | Female | 64 YR | 2047 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF | GM |
GM01652 | Female | 11 YR | 165 | proband | APPARENTLY HEALTHY INDIVIDUAL | GM |
GM03021 | Female | 17 YR | 1238 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG | GM |
GM09943 | Female | 7 YR | 1141 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC | GM |
GM03377 | Male | 19 YR | | proband | APPARENTLY HEALTHY INDIVIDUAL | GM |
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