Matches in DBpedia 2016-04 for { <https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1682672> ?p ?o }
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- PMC1682672 first1 "A.".
- PMC1682672 first10 "D. J.".
- PMC1682672 first11 "M.".
- PMC1682672 first12 "D.".
- PMC1682672 first13 "H.".
- PMC1682672 first14 "V.".
- PMC1682672 first15 "M.".
- PMC1682672 first16 "N.".
- PMC1682672 first17 "M. J.".
- PMC1682672 first18 "M.".
- PMC1682672 first19 "E. K.".
- PMC1682672 first2 "T. M.".
- PMC1682672 first20 "C.".
- PMC1682672 first21 "A.".
- PMC1682672 first22 "S. M.".
- PMC1682672 first23 "P.".
- PMC1682672 first24 "M. A.".
- PMC1682672 first25 "A.".
- PMC1682672 first26 "J.".
- PMC1682672 first27 "M.".
- PMC1682672 first28 "J.".
- PMC1682672 first29 "U.".
- PMC1682672 first3 "B. J.".
- PMC1682672 first30 "T.".
- PMC1682672 first4 "M.".
- PMC1682672 first5 "H.".
- PMC1682672 first6 "P.".
- PMC1682672 first7 "L. C.".
- PMC1682672 first8 "I.".
- PMC1682672 first9 "M.".
- PMC1682672 isCitedBy Single-nucleotide_polymorphism.
- PMC1682672 issue "2".
- PMC1682672 journal "American Journal of Human Genetics".
- PMC1682672 last1 "Hamosh".
- PMC1682672 last10 "Brock".
- PMC1682672 last11 "Macek".
- PMC1682672 last12 "Zemková".
- PMC1682672 last13 "Krásničanová".
- PMC1682672 last14 "Vávrová".
- PMC1682672 last15 "Macek".
- PMC1682672 last16 "Golder".
- PMC1682672 last17 "Schwarz".
- PMC1682672 last18 "Super".
- PMC1682672 last19 "Watson".
- PMC1682672 last2 "King".
- PMC1682672 last20 "Williams".
- PMC1682672 last21 "Bush".
- PMC1682672 last22 "O'Mahoney".
- PMC1682672 last23 "Humphries".
- PMC1682672 last24 "Dearce".
- PMC1682672 last25 "Reis".
- PMC1682672 last26 "Bürger".
- PMC1682672 last27 "Stuhrmann".
- PMC1682672 last28 "Schmidtke".
- PMC1682672 last29 "Wulbrand".
- PMC1682672 last3 "Rosenstein".
- PMC1682672 last30 "Dörk".
- PMC1682672 last4 "Corey".
- PMC1682672 last5 "Levison".
- PMC1682672 last6 "Durie".
- PMC1682672 last7 "Tsui".
- PMC1682672 last8 "McIntosh".
- PMC1682672 last9 "Keston".
- PMC1682672 pages "245–250".
- PMC1682672 pmc "1682672".
- PMC1682672 pmid "1379413".
- PMC1682672 title "Cystic fibrosis patients bearing both the common missense mutation Gly----Asp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileus".
- PMC1682672 volume "51".
- PMC1682672 year "1992".