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- s00439-005-1310-3 doi "10.1007/s00439-005-1310-3".
- s00439-005-1310-3 isCitedBy FOXG1.
- s00439-005-1310-3 issue "6".
- s00439-005-1310-3 journal "Hum. Genet.".
- s00439-005-1310-3 pages "536–44".
- s00439-005-1310-3 pmid "16133170".
- s00439-005-1310-3 title "Haploinsufficiency of novel FOXG1B variants in a patient with severe mental retardation, brain malformations and microcephaly".
- s00439-005-1310-3 vauthors "Shoichet SA, Kunde SA, Viertel P, Schell-Apacik C, von Voss H, Tommerup N, Ropers HH, Kalscheuer VM".
- s00439-005-1310-3 volume "117".
- s00439-005-1310-3 year "2005".