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- 1098-1004(200012)16:63.0.CO;2-V author "Morisaki H, Higuchi I, Abe M".
- 1098-1004(200012)16:63.0.CO;2-V author "Wijmenga C, Hansen RS, Gimelli G".
- 1098-1004(200012)16:63.0.CO;2-V displayAuthors "etal".
- 1098-1004(200012)16:63.0.CO;2-V doi "10.1002/1098-100416:63.0.CO;2-V".
- 1098-1004(200012)16:63.0.CO;2-V isCitedBy AMP_deaminase.
- 1098-1004(200012)16:63.0.CO;2-V isCitedBy DNMT3B.
- 1098-1004(200012)16:63.0.CO;2-V issue "6".
- 1098-1004(200012)16:63.0.CO;2-V journal "Hum. Mutat.".
- 1098-1004(200012)16:63.0.CO;2-V pages "467–72".
- 1098-1004(200012)16:63.0.CO;2-V pages "509–17".
- 1098-1004(200012)16:63.0.CO;2-V pmid "11102975".
- 1098-1004(200012)16:63.0.CO;2-V pmid "11102980".
- 1098-1004(200012)16:63.0.CO;2-V title "First missense mutations of AMPD1 accompanied with myopathy found in a Japanese patient.".
- 1098-1004(200012)16:63.0.CO;2-V title "Genetic variation in ICF syndrome: evidence for genetic heterogeneity.".
- 1098-1004(200012)16:63.0.CO;2-V volume "16".
- 1098-1004(200012)16:63.0.CO;2-V year "2001".