Publication

Emmert S, Slor H, Busch DB, Batko S, Albert RB, Coleman D, Khan SG, Abu-Libdeh B, DiGiovanna JJ, Cunningham BB, Lee MM, Crollick J, Inui H, Ueda T, Hedayati M, Grossman L, Shahlavi T, Cleaver JE, Kraemer KH, Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group g patients. J Invest Dermatol118(6):972-82 2002
PubMed ID: 12060391

Records Return:  (11) Show
 
Catalog IDGenderAge at SamplingFamilyRelationshipDescription
GM03651Female25 YR3029probandAPPARENTLY HEALTHY NON-FETAL TISSUE
AG08803Male1 YR2093probandXERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG
GM16023Female43 YR1823motherXERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG
GM16398Female13 YR1823probandXERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG
GM16464Male 1823fatherXERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG
GM00637Female18 YR162probandSV40 VIRUS-TRANSFORMED APPARENTLY HEALTHY: NON-FETAL TISSUE
GM11551Female16 YR1411probandCOCKAYNE SYNDROME TYPE UNSPECIFIED
GM16180Female  probandXERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG
GM16181Female  probandXERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG
AG06239Male59 YR probandGERONTOLOGY RESEARCH CENTER (GRC) CELL CULTURE COLLECTION
GM03377Male19 YR probandAPPARENTLY HEALTHY NON-FETAL TISSUE