Matches in DBpedia 2016-04 for { <http://doi.org/10.1038/ng1858> ?p ?o }
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- ng1858 author "Shaw-Smith C, Pittman AM, Willatt L".
- ng1858 author "Shaw-Smith C, Pittman AM, Willatt L, Martin H, Rickman L, Gribble S, Curley R, Cumming S, Dunn C, Kalaitzopoulos D, Porter K, Prigmore E, Krepischi-Santos AC, Varela MC, Koiffmann CP, Lees AJ, Rosenberg C, Firth HV, de Silva R, Carter NP".
- ng1858 author "Shaw-Smith, C; Pittman, Am; Willatt, L; Martin, H; Rickman, L; Gribble, S; Curley, R; Cumming, S; Dunn, C; Kalaitzopoulos, D; Porter, K; Prigmore, E; Krepischi-Santos, Ac; Varela, Mc; Koiffmann, Cp; Lees, Aj; Rosenberg, C; Firth, Hv; De, Silva, R; Carter, Np".
- ng1858 date "September 2006".
- ng1858 displayAuthors "etal".
- ng1858 doi "10.1038/ng1858".
- ng1858 isCitedBy 17q21.31_microdeletion_syndrome.
- ng1858 isCitedBy DECIPHER.
- ng1858 isCitedBy Genetic_history_of_Europe.
- ng1858 isCitedBy Tau_protein.
- ng1858 issn "1061-4036".
- ng1858 issue "9".
- ng1858 journal "Nat Genet".
- ng1858 journal "Nat. Genet.".
- ng1858 journal "Nature Genetics".
- ng1858 pages "1032–7".
- ng1858 pmid "16906163".
- ng1858 title "Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability".
- ng1858 title "Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability.".
- ng1858 vauthors "Shaw-Smith C, Pittman AM, Willatt L, Martin H, Rickman L, Gribble S, Curley R, Cumming S, Dunn C, Kalaitzopoulos D, Porter K, Prigmore E, Krepischi-Santos AC, Varela MC, Koiffmann CP, Lees AJ, Rosenberg C, Firth HV, de Silva R, Carter NP".
- ng1858 volume "38".
- ng1858 year "2006".