Matches in DBpedia 2016-04 for { <http://doi.org/10.1093/hmg/10.22.2539> ?p ?o }
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- 10.22.2539 displayauthors "8".
- 10.22.2539 doi "10.1093/hmg/10.22.2539".
- 10.22.2539 first1 "B. C.".
- 10.22.2539 first2 "M".
- 10.22.2539 first3 "H".
- 10.22.2539 first4 "EM".
- 10.22.2539 first5 "CF".
- 10.22.2539 first6 "T".
- 10.22.2539 first7 "M".
- 10.22.2539 first8 "E".
- 10.22.2539 first9 "VH".
- 10.22.2539 isCitedBy Progeroid_syndromes.
- 10.22.2539 issue "22".
- 10.22.2539 journal "Human Molecular Genetics".
- 10.22.2539 last1 "Broughton".
- 10.22.2539 last2 "Berneburg".
- 10.22.2539 last3 "Fawcett".
- 10.22.2539 last4 "Taylor".
- 10.22.2539 last5 "Arlett".
- 10.22.2539 last6 "Nardo".
- 10.22.2539 last7 "Stefanini".
- 10.22.2539 last8 "Menefee".
- 10.22.2539 last9 "Price".
- 10.22.2539 pages "2539–47".
- 10.22.2539 pmid "11709541".
- 10.22.2539 title "Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene".
- 10.22.2539 volume "10".
- 10.22.2539 year "2001".